A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661972



Internal ID15051938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:141608987..141671175hg38UCSC Ensembl
InnerchrX:140697115..140759327hg19UCSC Ensembl
InnerchrX:140524781..140586993hg18UCSC Ensembl
InnerchrX:140422635..140484847hg17UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3862189
hg1962213
hg1862213
hg1762213
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516880
Supporting Variants
Samples
Known GenesSPANXA2-OT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661972
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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