A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230080



Internal ID20797120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6992077..7044384hg38UCSC Ensembl
chr6:6992310..7044617hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3852308
hg1952308
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405767
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230080
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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