A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18057699



Internal ID20624739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212646496..212653569hg38UCSC Ensembl
chr1:212819838..212826911hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg387074
hg197074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330585
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18057699
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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