A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18149084



Internal ID20716124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87261001..87264200hg38UCSC Ensembl
chr6:87970719..87973918hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6400322
Supporting Variants
Samples
Known GenesZNF292
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18149084
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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