A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358984



Internal ID21016537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160395997..160399027hg38UCSC Ensembl
chr3:160113785..160116815hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg383031
hg193031
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094765
Samples
Known GenesIFT80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358984
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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