A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669029



Internal ID15058995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:134547388..134576106hg38UCSC Ensembl
InnerchrX:133681418..133710136hg19UCSC Ensembl
InnerchrX:133509084..133537802hg18UCSC Ensembl
InnerchrX:133406938..133435656hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3828719
hg1928719
hg1828719
hg1728719
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517076
Supporting Variants
Samples
Known GenesLINC00629, PLAC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669029
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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