A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613882



Internal ID7000777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81156372..81158116hg38UCSC Ensembl
Innerchr7:81156391..81158098hg38UCSC Ensembl
Outerchr7:81156354..81158135hg38UCSC Ensembl
chr7:80785688..80787432hg19UCSC Ensembl
Innerchr7:80785707..80787414hg19UCSC Ensembl
Outerchr7:80785670..80787451hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg381745
hg191745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12864802, essv12864803
SamplesHG01485, HG03198
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613882
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