A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355706



Internal ID21013259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155532777..155534529hg38UCSC Ensembl
chr3:155250566..155252318hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg381753
hg191753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096430
Samples
Known GenesPLCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355706
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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