A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517076



Internal ID15097683
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 StatusM
Merged Variants
Supporting Variantsnssv652127, nssv653739, nssv657063, nssv674671, nssv669029, nssv669292, nssv665962, nssv651840
Samples
Known GenesLINC00629, PLAC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517076
Frequency
Sample Size2026
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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