A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668609



Internal ID15405261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:33375052..33503133hg38UCSC Ensembl
InnerchrX:33393169..33521250hg19UCSC Ensembl
InnerchrX:33303090..33431171hg18UCSC Ensembl
InnerchrX:33152826..33280907hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38128082
hg19128082
hg18128082
hg17128082
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516480
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668609
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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