A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360932



Internal ID21018485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150915437..150916219hg38UCSC Ensembl
chr3:150633224..150634006hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38783
hg19783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096589
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360932
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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