A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697781



Internal ID15434433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:95709071..95739227hg38UCSC Ensembl
Innerchr11:95442235..95472391hg19UCSC Ensembl
Innerchr11:95081883..95112039hg18UCSC Ensembl
Innerchr11:95081883..95112039hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3830157
hg1930157
hg1830157
hg1730157
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521090
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697781
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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