A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217031



Internal ID20784071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165763301..165767500hg38UCSC Ensembl
chr6:166176789..166180988hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613203
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217031
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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