A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18050792



Internal ID20617832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106800561..106836231hg38UCSC Ensembl
chr1:107343183..107378853hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3835671
hg1935671
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327693
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18050792
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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