A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419136



Internal ID22477006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196199732..196201510hg38UCSC Ensembl
chr3:195926603..195928381hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381779
hg191779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906246
Supporting Variants
Samples
Known GenesZDHHC19
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419136
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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