A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17429043



Internal ID22486913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36514209..36515966hg38UCSC Ensembl
chr3:36555701..36557458hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg381758
hg191758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5895440
Supporting Variants
Samples
Known GenesSTAC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17429043
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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