A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516078



Internal ID15443371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:101415002..101419220hg38UCSC Ensembl
Innerchr13:102067353..102071571hg19UCSC Ensembl
Innerchr13:100865354..100869572hg18UCSC Ensembl
Innerchr13:100865354..100869572hg17UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg384219
hg194219
hg184219
hg174219
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv666045, nssv681117
Samples
Known GenesNALCN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516078
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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