A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687571



Internal ID15077537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:30321210..30418090hg38UCSC Ensembl
InnerchrX:30339327..30436207hg19UCSC Ensembl
InnerchrX:30249248..30346128hg18UCSC Ensembl
InnerchrX:30098984..30195864hg17UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3896881
hg1996881
hg1896881
hg1796881
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520655
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687571
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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