A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15194762



Internal ID21333660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77977678..77977678hg38UCSC Ensembl
chr13:78551813..78551813hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3944034
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15194762
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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