A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703519



Internal ID15440171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:140804585..140838818hg38UCSC Ensembl
InnerchrX:139886750..139920983hg19UCSC Ensembl
InnerchrX:139714416..139748649hg18UCSC Ensembl
InnerchrX:139612270..139646503hg17UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3834234
hg1934234
hg1834234
hg1734234
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527132
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703519
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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