A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141082



Internal ID20708122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:141772476..142005840hg38UCSC Ensembl
chr6:142093613..142326977hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38233365
hg19233365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619778
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141082
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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