A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202842



Internal ID20769882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25426401..25434500hg38UCSC Ensembl
chr1:25752892..25760991hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg388100
hg198100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317623
Supporting Variants
Samples
Known GenesTMEM57
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202842
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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