A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231740



Internal ID20798780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36253033..36383991hg38UCSC Ensembl
chr6:36220810..36351768hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38130959
hg19130959
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407975
Supporting Variants
Samples
Known GenesC6orf222, ETV7, PNPLA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231740
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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