A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423078



Internal ID22480948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:143221503..143221604hg38UCSC Ensembl
chr5:142601068..142601169hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905095
Supporting Variants
Samples
Known GenesARHGAP26
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423078
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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