A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359232



Internal ID21016785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64430407..64432305hg38UCSC Ensembl
chr3:64416083..64417981hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381899
hg191899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101500
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359232
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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