A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691178



Internal ID15427830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:8969712..8995599hg38UCSC Ensembl
InnerchrX:8937753..8963640hg19UCSC Ensembl
InnerchrX:8897753..8923640hg18UCSC Ensembl
InnerchrX:8747489..8773376hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3825888
hg1925888
hg1825888
hg1725888
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)nssv691178
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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