A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696106



Internal ID15432758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:84510546..84515729hg38UCSC Ensembl
InnerchrX:83765554..83770737hg19UCSC Ensembl
InnerchrX:83652210..83657393hg18UCSC Ensembl
InnerchrX:83571699..83576882hg17UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg385184
hg195184
hg185184
hg175184
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520647
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696106
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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