A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695211



Internal ID15085177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2614158..2623904hg38UCSC Ensembl
Innerchr7:2653792..2663538hg19UCSC Ensembl
Innerchr7:2620318..2630064hg18UCSC Ensembl
Innerchr7:2427033..2436779hg17UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg389747
hg199747
hg189747
hg179747
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517403
Supporting Variants
Samples
Known GenesIQCE
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695211
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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