A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196984



Internal ID20764024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64505923..64508542hg38UCSC Ensembl
chr15:64798122..64800741hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg382620
hg192620
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502862
Supporting Variants
Samples
Known GenesZNF609
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196984
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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