A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359096



Internal ID21016649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138264758..138264824hg38UCSC Ensembl
chr3:137983600..137983666hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093883
Samples
Known GenesARMC8, NME9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359096
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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