A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368408



Internal ID21025961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62678723..62709990hg38UCSC Ensembl
chr3:62664398..62695665hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3831268
hg1931268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101791
Samples
Known GenesCADPS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368408
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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