A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613008



Internal ID6999906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44377882..44379959hg38UCSC Ensembl
Innerchr7:44377885..44379957hg38UCSC Ensembl
Outerchr7:44377880..44379962hg38UCSC Ensembl
chr7:44417481..44419558hg19UCSC Ensembl
Innerchr7:44417484..44419556hg19UCSC Ensembl
Outerchr7:44417479..44419561hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382078
hg192078
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12756619, essv12756614, essv12756612, essv12756618, essv12756621, essv12756616, essv12756617, essv12756622, essv12756613, essv12756615, essv12756620
SamplesNA19204, HG02804, HG02811, NA19210, HG03563, HG03472, HG03382, HG02309, HG03571, HG03899, HG03442
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613008
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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