A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661891



Internal ID15051857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:38631591..38797404hg38UCSC Ensembl
InnerchrX:38490844..38656657hg19UCSC Ensembl
InnerchrX:38375788..38541601hg18UCSC Ensembl
InnerchrX:38247061..38412875hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38165814
hg19165814
hg18165814
hg17165815
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520210
Supporting Variants
Samples
Known GenesTSPAN7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661891
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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