A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527943



Internal ID15455236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:33924785..33932609hg38UCSC Ensembl
Innerchr13:34498922..34506746hg19UCSC Ensembl
Innerchr13:33396922..33404746hg18UCSC Ensembl
Innerchr13:33396922..33404746hg17UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg387825
hg197825
hg187825
hg177825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704451
Samples
Known GenesRFC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527943
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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