A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685749



Internal ID15075715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:38631591..38769214hg38UCSC Ensembl
InnerchrX:38490844..38628467hg19UCSC Ensembl
InnerchrX:38375788..38513411hg18UCSC Ensembl
InnerchrX:38247061..38384685hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38137624
hg19137624
hg18137624
hg17137625
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)nssv685749
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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