A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060974



Internal ID20628014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33481657..33481986hg38UCSC Ensembl
chr1:33947257..33947586hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334933
Supporting Variants
Samples
Known GenesZSCAN20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060974
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00143


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