A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612696



Internal ID6999596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29598323..29606430hg38UCSC Ensembl
Innerchr7:29598323..29606430hg38UCSC Ensembl
Outerchr7:29598181..29606558hg38UCSC Ensembl
chr7:29637939..29646046hg19UCSC Ensembl
Innerchr7:29637939..29646046hg19UCSC Ensembl
Outerchr7:29637797..29646174hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg388108
hg198108
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12717351, essv12717350
SamplesHG02675, HG02654
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612696
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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