A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683661



Internal ID15420313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:70546008..70819919hg38UCSC Ensembl
InnerchrX:69765858..70039769hg19UCSC Ensembl
InnerchrX:69682583..69956494hg18UCSC Ensembl
InnerchrX:69548879..69822790hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38273912
hg19273912
hg18273912
hg17273912
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517078
Supporting Variants
Samples
Known GenesTEX11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683661
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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