A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520427



Internal ID15447720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:62709286..62954651hg38UCSC Ensembl
InnerchrX:61928756..62174121hg19UCSC Ensembl
InnerchrX:61845481..62090846hg18UCSC Ensembl
InnerchrX:61711777..61957142hg17UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg38245366
hg19245366
hg18245366
hg17245366
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv683721, nssv677076, nssv671363, nssv691577, nssv687917
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520427
Frequency
Sample Size2026
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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