A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677350



Internal ID15414002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:116808832..116905365hg38UCSC Ensembl
InnerchrX:115942800..116039333hg19UCSC Ensembl
InnerchrX:115826828..115923361hg18UCSC Ensembl
InnerchrX:115724682..115821215hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3896534
hg1996534
hg1896534
hg1796534
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516826
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677350
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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