A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613630



Internal ID6653839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71494059..71494762hg38UCSC Ensembl
Innerchr7:71494060..71494762hg38UCSC Ensembl
Outerchr7:71494059..71494763hg38UCSC Ensembl
chr7:70959044..70959747hg19UCSC Ensembl
Innerchr7:70959045..70959747hg19UCSC Ensembl
Outerchr7:70959044..70959748hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38704
hg19704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12829709, essv12829711, essv12829706, essv12829707, essv12829710, essv12829708
SamplesNA12827, HG01605, HG01182, HG01392, HG01183, HG01102
Known GenesWBSCR17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613630
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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