A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695229



Internal ID15431881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:140804585..140844602hg38UCSC Ensembl
InnerchrX:139886750..139926767hg19UCSC Ensembl
InnerchrX:139714416..139754433hg18UCSC Ensembl
InnerchrX:139612270..139652287hg17UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3840018
hg1940018
hg1840018
hg1740018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517824
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695229
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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