A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360905



Internal ID21018458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:174747629..174751415hg38UCSC Ensembl
chr3:174465419..174469205hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg383787
hg193787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097503
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360905
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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