A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689192



Internal ID15079158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:141431353..141460613hg38UCSC Ensembl
InnerchrX:140519367..140548607hg19UCSC Ensembl
InnerchrX:140347033..140376273hg18UCSC Ensembl
InnerchrX:140244887..140274127hg17UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3829261
hg1929241
hg1829241
hg1729241
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516880
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689192
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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