A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493743



Internal ID22551673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117813828..117859370hg38UCSC Ensembl
chr5:117149523..117195065hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3845543
hg1945543
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840712
Supporting Variants
Samples
Known GenesLOC102467224
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493743
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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