A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216700



Internal ID20783740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157405400..157410903hg38UCSC Ensembl
chr6:157826432..157831935hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg385504
hg195504
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6601788
Supporting Variants
Samples
Known GenesZDHHC14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216700
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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