A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613624



Internal ID6653833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71211293..71213231hg38UCSC Ensembl
Innerchr7:71211293..71213231hg38UCSC Ensembl
Outerchr7:71210905..71213627hg38UCSC Ensembl
chr7:70676279..70678217hg19UCSC Ensembl
Innerchr7:70676279..70678217hg19UCSC Ensembl
Outerchr7:70675891..70678613hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg381939
hg191939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12829563, essv12829564, essv12829565, essv12829568, essv12829566, essv12829567
SamplesHG00864, HG00475, HG01867, HG00663, NA18548, HG00708
Known GenesWBSCR17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613624
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer