A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216731



Internal ID20783771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160507360..160661249hg38UCSC Ensembl
chr6:160928392..161082281hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38153890
hg19153890
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600879
Supporting Variants
Samples
Known GenesLPA, LPAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216731
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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