A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356033



Internal ID21013586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132998701..133006000hg38UCSC Ensembl
chr3:132717545..132724844hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg387300
hg197300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5026n223
Supporting Variantsnssv18094203
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356033
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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