A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427329



Internal ID22485199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69089593..69090984hg38UCSC Ensembl
chr3:69138744..69140135hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381392
hg191392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897981
Supporting Variants
Samples
Known GenesARL6IP5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427329
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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