A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520792



Internal ID20894153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36610627..36661034hg38UCSC Ensembl
chr19:37101529..37151936hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3850408
hg1950408
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197817
Samples
Known GenesZNF382, ZNF461
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520792
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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