A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656256



Internal ID15392908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:50408411..50418611hg38UCSC Ensembl
Innerchr7:50476109..50486309hg19UCSC Ensembl
Innerchr7:50443603..50453803hg18UCSC Ensembl
Innerchr7:50250318..50260518hg17UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg3810201
hg1910201
hg1810201
hg1710201
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515738
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656256
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