A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698082



Internal ID15434734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:69723837..69907713hg38UCSC Ensembl
InnerchrX:68943681..69127562hg19UCSC Ensembl
InnerchrX:68860406..69044287hg18UCSC Ensembl
InnerchrX:68726702..68910583hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38183877
hg19183882
hg18183882
hg17183882
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521471
Supporting Variants
Samples
Known GenesEDA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698082
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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