A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614283



Internal ID7001178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99805270..99809354hg38UCSC Ensembl
Innerchr7:99805270..99809354hg38UCSC Ensembl
Outerchr7:99804770..99809854hg38UCSC Ensembl
chr7:99402893..99406977hg19UCSC Ensembl
Innerchr7:99402893..99406977hg19UCSC Ensembl
Outerchr7:99402393..99407477hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg384085
hg194085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12908558, essv12908559, essv12908557
SamplesNA19055, NA18647, NA18957
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614283
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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