A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705672



Internal ID21377948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101241793..101244073hg38UCSC Ensembl
chr13:101894144..101896424hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg382281
hg192281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390822
Supporting Variants
Samples
Known GenesNALCN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705672
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.278736


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