A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177282



Internal ID20744322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66541016..66542324hg38UCSC Ensembl
chr15:66833354..66834662hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381309
hg191309
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506110
Supporting Variants
Samples
Known GenesZWILCH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177282
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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