A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697296



Internal ID15433948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:44562040..44575014hg38UCSC Ensembl
InnerchrX:44421286..44434260hg19UCSC Ensembl
InnerchrX:44306230..44319204hg18UCSC Ensembl
InnerchrX:44177540..44190514hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3812975
hg1912975
hg1812975
hg1712975
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520232
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697296
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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