A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700043



Internal ID15436695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:8087457..8469952hg38UCSC Ensembl
InnerchrX:8055498..8437993hg19UCSC Ensembl
InnerchrX:8015498..8397993hg18UCSC Ensembl
InnerchrX:7865234..8247729hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38382496
hg19382496
hg18382496
hg17382496
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524164
Supporting Variants
Samples
Known GenesMIR651, VCX2, VCX3B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700043
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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