A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373604



Internal ID21031157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38696470..38697878hg38UCSC Ensembl
chr3:38737961..38739369hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg381409
hg191409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100843
Samples
Known GenesSCN10A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373604
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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