A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15201881



Internal ID21340686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2940605..2940605hg38UCSC Ensembl
chr6:2940839..2940839hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3941007
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15201881
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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