A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052977



Internal ID20620017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150599584..150601888hg38UCSC Ensembl
chr1:150572060..150574364hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg382305
hg192305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318162
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052977
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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