A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18063186



Internal ID20630226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77073101..77075000hg38UCSC Ensembl
chr1:77538786..77540685hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329788
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18063186
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00152


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