A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18134639



Internal ID20701679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104526918..104549197hg38UCSC Ensembl
chr6:104974793..104997072hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3822280
hg1922280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607074
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18134639
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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