A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18058900



Internal ID20625940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:236004394..236006618hg38UCSC Ensembl
chr1:236167694..236169918hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg382225
hg192225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322410
Supporting Variants
Samples
Known GenesNID1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18058900
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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