A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497448



Internal ID22555382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60529161..60534561hg38UCSC Ensembl
chr5:59824988..59830388hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg385401
hg195401
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842824
Supporting Variants
Samples
Known GenesPART1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497448
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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