A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698080



Internal ID15088046
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 StatusS
Merged Variantsnsv521470
Supporting Variants
Samples
Known GenesLINC00629, PLAC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698080
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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