A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357330



Internal ID21014883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101581873..101583694hg38UCSC Ensembl
chr3:101300717..101302538hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg381822
hg191822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092406
Samples
Known GenesPCNP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357330
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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