A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374504



Internal ID21032057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:102461012..102580308hg38UCSC Ensembl
chr3:102179856..102299152hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38119297
hg19119297
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208895
Samples
Known GenesZPLD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374504
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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