A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202551



Internal ID20769591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25086404..25496168hg38UCSC Ensembl
chr20:25067040..25476804hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38409765
hg19409765
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532719
Supporting Variants
Samples
Known GenesABHD12, ENTPD6, GINS1, LOC284798, NINL, PYGB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202551
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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