A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373387



Internal ID21030940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155638555..155642710hg38UCSC Ensembl
chr3:155356344..155360499hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg384156
hg194156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096436
Samples
Known GenesPLCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373387
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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