A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671508



Internal ID15408160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5688580..5748288hg38UCSC Ensembl
InnerchrX:5606621..5666329hg19UCSC Ensembl
InnerchrX:5616621..5676329hg18UCSC Ensembl
InnerchrX:5466357..5526065hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3859709
hg1959709
hg1859709
hg1759709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515922
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671508
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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