A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608816



Internal ID20981887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157383833..157384897hg38UCSC Ensembl
chr6:157804865..157805929hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg381065
hg191065
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141941
Samples
Known GenesZDHHC14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608816
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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