A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706003



Internal ID15095969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:94772808..94964713hg38UCSC Ensembl
InnerchrX:94027807..94219712hg19UCSC Ensembl
InnerchrX:93914463..94106368hg18UCSC Ensembl
InnerchrX:93833952..94025857hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38191906
hg19191906
hg18191906
hg17191906
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)nssv706003
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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