A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704176



Internal ID15440828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:4830956..4933015hg38UCSC Ensembl
InnerchrX:4748997..4851056hg19UCSC Ensembl
InnerchrX:4758997..4861056hg18UCSC Ensembl
InnerchrX:4608733..4710792hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg38102060
hg19102060
hg18102060
hg17102060
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527698
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704176
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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