A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526744



Internal ID15454037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:104772195..104794962hg38UCSC Ensembl
Innerchr13:105424546..105447313hg19UCSC Ensembl
Innerchr13:104222547..104245314hg18UCSC Ensembl
Innerchr13:104222547..104245314hg17UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3822768
hg1922768
hg1822768
hg1722768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703088
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526744
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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