A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360345



Internal ID21017898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72171128..72172659hg38UCSC Ensembl
chr3:72220279..72221810hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381532
hg191532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103781
Samples
Known GenesLINC00870
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360345
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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