A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595770



Internal ID6636044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32297309..32298230hg38UCSC Ensembl
Innerchr3:32297342..32298197hg38UCSC Ensembl
Outerchr3:32297276..32298263hg38UCSC Ensembl
chr3:32338801..32339722hg19UCSC Ensembl
Innerchr3:32338834..32339689hg19UCSC Ensembl
Outerchr3:32338768..32339755hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38922
hg19922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10975031, essv10975016, essv10975014, essv10975027, essv10975038, essv10975025, essv10975026, essv10975019, essv10975012, essv10975017, essv10975041, essv10975023, essv10975036, essv10975010, essv10975033, essv10975045, essv10975022, essv10975035, essv10975039, essv10975030, essv10975011, essv10975046, essv10975034, essv10975020, essv10975018, essv10975048, essv10975029, essv10975042, essv10975047, essv10975015, essv10975024, essv10975040, essv10975044, essv10975043, essv10975032, essv10975013, essv10975037, essv10975021, essv10975028
SamplesNA12814, HG04158, NA12045, HG00181, HG01704, HG01522, HG00337, HG02407, NA20795, HG00736, NA07347, NA20759, NA12156, HG00309, NA20811, NA12748, HG01524, HG00282, HG01515, NA20536, HG02108, NA20767, HG01092, HG01504, HG01383, HG00117, NA20799, NA19440, HG01357, HG01174, NA20792, HG00256, HG02238, HG01631, NA20758, HG04171, NA20502, HG01756, HG01516
Known GenesCMTM8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595770
Frequency
Sample Size2504
Observed Gain0
Observed Loss39
Observed Complex0
Frequencyn/a


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