A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703011



Internal ID15439663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:79889943..79938107hg38UCSC Ensembl
InnerchrX:79145448..79193603hg19UCSC Ensembl
InnerchrX:79032104..79080259hg18UCSC Ensembl
InnerchrX:78951593..78999748hg17UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3848165
hg1948156
hg1848156
hg1748156
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526679
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703011
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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