A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685411



Internal ID15075377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:94464258..94989222hg38UCSC Ensembl
InnerchrX:93719257..94244221hg19UCSC Ensembl
InnerchrX:93605913..94130877hg18UCSC Ensembl
InnerchrX:93525402..94050366hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38524965
hg19524965
hg18524965
hg17524965
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519792
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv685411
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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