A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364247



Internal ID21021800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16436770..16482842hg38UCSC Ensembl
chr3:16478277..16524349hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3846073
hg1946073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095542
Samples
Known GenesRFTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364247
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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