A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898860



Internal ID22673983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60517549..60517618hg38UCSC Ensembl
chr5:59813376..59813445hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415333
Samples
Known GenesPART1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898860
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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