A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701659



Internal ID15091625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:141260298..141292021hg38UCSC Ensembl
InnerchrX:140354434..140386165hg19UCSC Ensembl
InnerchrX:140182100..140213831hg18UCSC Ensembl
InnerchrX:140079954..140111685hg17UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3831724
hg1931732
hg1831732
hg1731732
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)nssv701659
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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