A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18056996



Internal ID20624036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20404942..20406813hg38UCSC Ensembl
chr1:20731435..20733306hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg381872
hg191872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327848
Supporting Variants
Samples
Known GenesLINC01141
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18056996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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