A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060705



Internal ID20627745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35740740..35742014hg38UCSC Ensembl
chr1:36206341..36207615hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381275
hg191275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322137
Supporting Variants
Samples
Known GenesCLSPN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060705
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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