A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18063819



Internal ID20630859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:73631774..73632220hg38UCSC Ensembl
chr1:74097457..74097903hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331977
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18063819
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00067


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