A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140288



Internal ID20707328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144603721..144604352hg38UCSC Ensembl
chr6:144924857..144925488hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38632
hg19632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612713
Supporting Variants
Samples
Known GenesUTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140288
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00028


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