A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361001



Internal ID21018554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99027824..99085713hg38UCSC Ensembl
chr3:98746668..98804557hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3857890
hg1957890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104966
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361001
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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