A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17424013



Internal ID22481883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42962141..43046337hg38UCSC Ensembl
chr5:42962243..43046439hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3884197
hg1984197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5893425
Supporting Variants
Samples
Known GenesANXA2R, FLJ32255, LOC153684, LOC648987
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17424013
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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