A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527697



Internal ID15454990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:44055446..44085467hg38UCSC Ensembl
InnerchrX:43914692..43944713hg19UCSC Ensembl
InnerchrX:43799636..43829657hg18UCSC Ensembl
InnerchrX:43670946..43700967hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3830022
hg1930022
hg1830022
hg1730022
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704175
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527697
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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