A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15201915



Internal ID21340717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13925069..13925069hg38UCSC Ensembl
chr6:13925300..13925300hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3950750
Supporting Variants
SamplesHG002
Known GenesRNF182
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15201915
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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