A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695444



Internal ID15432096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:113117141..113121995hg38UCSC Ensembl
InnerchrX:112360369..112365223hg19UCSC Ensembl
InnerchrX:112247025..112251879hg18UCSC Ensembl
InnerchrX:112166514..112171368hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg384855
hg194855
hg184855
hg174855
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515695
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695444
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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