A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064621



Internal ID20631661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:95662601..95663741hg38UCSC Ensembl
chr1:96128157..96129297hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg381141
hg191141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332360
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064621
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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