A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613560



Internal ID7000456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67752456..67757970hg38UCSC Ensembl
Innerchr7:67752470..67757956hg38UCSC Ensembl
Outerchr7:67752442..67757984hg38UCSC Ensembl
chr7:67217443..67222957hg19UCSC Ensembl
Innerchr7:67217457..67222943hg19UCSC Ensembl
Outerchr7:67217429..67222971hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg385515
hg195515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12826527, essv12826526
SamplesNA19376, NA19430
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613560
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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