A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704002



Internal ID21376278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167784655..167784850hg38UCSC Ensembl
chr6:168185335..168185530hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392770
Supporting Variants
Samples
Known GenesC6orf123
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704002
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0172414


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