A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209613



Internal ID20776653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138048112..138126083hg38UCSC Ensembl
chr3:137766954..137844925hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3877972
hg1977972
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366209
Supporting Variants
Samples
Known GenesA4GNT, DZIP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209613
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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