A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698478



Internal ID15435130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:104431672..104448307hg38UCSC Ensembl
InnerchrX:103676353..103692988hg19UCSC Ensembl
InnerchrX:103563009..103579644hg18UCSC Ensembl
InnerchrX:103482498..103499133hg17UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3816636
hg1916636
hg1816636
hg1716636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522828
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698478
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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