A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598378



Internal ID6985514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160164387..160165289hg38UCSC Ensembl
Innerchr3:160164389..160165288hg38UCSC Ensembl
Outerchr3:160164386..160165291hg38UCSC Ensembl
chr3:159882174..159883076hg19UCSC Ensembl
Innerchr3:159882176..159883075hg19UCSC Ensembl
Outerchr3:159882173..159883078hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38903
hg19903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11199618, essv11199621, essv11199622, essv11199619, essv11199625, essv11199620, essv11199617, essv11199623, essv11199624, essv11199626, essv11199616
SamplesHG02583, HG02852, HG02798, NA18486, NA19355, HG02854, HG03024, HG02484, HG02722, HG02464, HG02771
Known GenesIL12A-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598378
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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