A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15202907



Internal ID21341710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161646345..161646345hg38UCSC Ensembl
chr6:162067377..162067377hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3937564
Supporting Variants
SamplesHG002
Known GenesPARK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15202907
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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