A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691201



Internal ID15427853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5688580..5742174hg38UCSC Ensembl
InnerchrX:5606621..5660215hg19UCSC Ensembl
InnerchrX:5616621..5670215hg18UCSC Ensembl
InnerchrX:5466357..5519951hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3853595
hg1953595
hg1853595
hg1753595
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)nssv691201
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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