A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17496721



Internal ID22554655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43013474..43045922hg38UCSC Ensembl
chr5:43013576..43046024hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3832449
hg1932449
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842429
Supporting Variants
Samples
Known GenesANXA2R, LOC153684, LOC648987
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17496721
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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