A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661055



Internal ID15397707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:8285491..8426212hg38UCSC Ensembl
InnerchrX:8253532..8394253hg19UCSC Ensembl
InnerchrX:8213532..8354253hg18UCSC Ensembl
InnerchrX:8063268..8203989hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38140722
hg19140722
hg18140722
hg17140722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516754
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661055
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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