A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15752981



Internal ID21387888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:53163019..53163771hg38UCSC Ensembl
chr5:52458849..52459601hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434660
Supporting Variants
SamplesMDQ045
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15752981
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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