A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358784



Internal ID21016337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81706402..81706838hg38UCSC Ensembl
chr3:81755553..81755989hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103176
Samples
Known GenesGBE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358784
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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