A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700289



Internal ID15436941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:100963177..101011605hg38UCSC Ensembl
Innerchr13:101615431..101663957hg19UCSC Ensembl
Innerchr13:100413432..100461958hg18UCSC Ensembl
Innerchr13:100413432..100461958hg17UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3848429
hg1948527
hg1848527
hg1748527
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524376
Supporting Variants
Samples
Known GenesNALCN-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700289
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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