A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669030



Internal ID15405682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:8956882..8976062hg38UCSC Ensembl
InnerchrX:8924923..8944103hg19UCSC Ensembl
InnerchrX:8884923..8904103hg18UCSC Ensembl
InnerchrX:8734659..8753839hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3819181
hg1919181
hg1819181
hg1719181
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515590
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669030
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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