A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526925



Internal ID15107532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:46178536..46180599hg38UCSC Ensembl
Innerchr13:46752671..46754734hg19UCSC Ensembl
Innerchr13:45650672..45652735hg18UCSC Ensembl
Innerchr13:45650672..45652735hg17UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg382064
hg192064
hg182064
hg172064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703289
Samples
Known GenesLCP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526925
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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