A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355862



Internal ID21013415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151781480..151786324hg38UCSC Ensembl
chr3:151499268..151504112hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg384845
hg194845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096644
Samples
Known GenesLOC201651, MIR548H2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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