A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137159



Internal ID20704199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116581801..116582500hg38UCSC Ensembl
chr6:116902964..116903663hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614318
Supporting Variants
Samples
Known GenesRWDD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137159
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00122


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