A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368604



Internal ID21026157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16754347..16774056hg38UCSC Ensembl
chr3:16795854..16815563hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3819710
hg1919710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098127
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368604
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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