A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696104



Internal ID15086070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:30321210..30371866hg38UCSC Ensembl
InnerchrX:30339327..30389983hg19UCSC Ensembl
InnerchrX:30249248..30299904hg18UCSC Ensembl
InnerchrX:30098984..30149640hg17UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3850657
hg1950657
hg1850657
hg1750657
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)nssv696104
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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