A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678902



Internal ID15415554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:8285230..8425685hg38UCSC Ensembl
InnerchrX:8253271..8393726hg19UCSC Ensembl
InnerchrX:8213271..8353726hg18UCSC Ensembl
InnerchrX:8063007..8203462hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38140456
hg19140456
hg18140456
hg17140456
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516754
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678902
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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