A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366482



Internal ID21024035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151957801..151976000hg38UCSC Ensembl
chr3:151675589..151693789hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3818200
hg1918201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096670
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366482
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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