A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615283



Internal ID7002172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142618728..142634741hg38UCSC Ensembl
Innerchr7:142618728..142634741hg38UCSC Ensembl
Outerchr7:142618728..142635241hg38UCSC Ensembl
chr7:142326224..142342257hg19UCSC Ensembl
Innerchr7:142326224..142342257hg19UCSC Ensembl
Outerchr7:142325724..142342757hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3816014
hg1916034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12987721, essv12987716, essv12987718, essv12987719, essv12987720, essv12987717
SamplesNA19350, HG02870, NA07347, HG01615, NA20282, HG02408
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615283
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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