A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521470



Internal ID15102077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:134547388..134609488hg38UCSC Ensembl
InnerchrX:133681418..133743518hg19UCSC Ensembl
InnerchrX:133509084..133571184hg18UCSC Ensembl
InnerchrX:133406938..133469038hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3862101
hg1962101
hg1862101
hg1762101
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698080
Samples
Known GenesLINC00629, PLAC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521470
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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