A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698554



Internal ID15435206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:140571102..140665347hg38UCSC Ensembl
InnerchrX:139653267..139747512hg19UCSC Ensembl
InnerchrX:139480933..139575178hg18UCSC Ensembl
InnerchrX:139378787..139473032hg17UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3894246
hg1994246
hg1894246
hg1794246
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522896
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698554
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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