A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373006



Internal ID21030559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71783901..71786400hg38UCSC Ensembl
chr3:71833052..71835551hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208693
Samples
Known GenesPROK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373006
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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