A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697293



Internal ID15433945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:116867930..116875777hg38UCSC Ensembl
InnerchrX:116001898..116009745hg19UCSC Ensembl
InnerchrX:115885926..115893773hg18UCSC Ensembl
InnerchrX:115783780..115791627hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg387848
hg197848
hg187848
hg177848
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
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)nssv697293
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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