A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370007



Internal ID21027560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:166985914..167087991hg38UCSC Ensembl
chr3:166703702..166805779hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38102078
hg19102078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370007
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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