A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062099



Internal ID20629139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60555825..60556395hg38UCSC Ensembl
chr1:61021497..61022067hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316503
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062099
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00058


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