A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612687



Internal ID6999587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29019673..29040170hg38UCSC Ensembl
Innerchr7:29019733..29040110hg38UCSC Ensembl
Outerchr7:29019613..29040230hg38UCSC Ensembl
chr7:29059289..29079786hg19UCSC Ensembl
Innerchr7:29059349..29079726hg19UCSC Ensembl
Outerchr7:29059229..29079846hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3820498
hg1920498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12716920, essv12716921
SamplesHG02130, HG02654
Known GenesCPVL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612687
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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