A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697544



Internal ID15434196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:113985318..113986808hg38UCSC Ensembl
InnerchrX:113228559..113230049hg19UCSC Ensembl
InnerchrX:113114824..113116314hg18UCSC Ensembl
InnerchrX:113034313..113035803hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg381491
hg191491
hg181491
hg171491
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515718
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697544
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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