A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096437



Internal ID20663477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155640901..155642000hg38UCSC Ensembl
chr3:155358690..155359789hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355992
Supporting Variants
Samples
Known GenesPLCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096437
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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