A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673464



Internal ID15063430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:94464258..94964713hg38UCSC Ensembl
InnerchrX:93719257..94219712hg19UCSC Ensembl
InnerchrX:93605913..94106368hg18UCSC Ensembl
InnerchrX:93525402..94025857hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38500456
hg19500456
hg18500456
hg17500456
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)nssv673464
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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