A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355907



Internal ID21013460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142822479..142826284hg38UCSC Ensembl
chr3:142541321..142545126hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg383806
hg193806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094372
Samples
Known GenesPCOLCE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355907
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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