A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375505



Internal ID21033058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:115760047..115768225hg38UCSC Ensembl
chr3:115478894..115487072hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg388179
hg198179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092894
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375505
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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