A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699923



Internal ID15089889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5810135..5879843hg38UCSC Ensembl
InnerchrX:5728176..5797884hg19UCSC Ensembl
InnerchrX:5738176..5807884hg18UCSC Ensembl
InnerchrX:5587912..5657620hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3869709
hg1969709
hg1869709
hg1769709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524057
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699923
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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