A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703698



Internal ID15440350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:93325927..93329679hg38UCSC Ensembl
InnerchrX:92580926..92584678hg19UCSC Ensembl
InnerchrX:92467582..92471334hg18UCSC Ensembl
InnerchrX:92387071..92390823hg17UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg383753
hg193753
hg183753
hg173753
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516563
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703698
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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