A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15747014



Internal ID21389746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:53163124..53163841hg38UCSC Ensembl
chr5:52458954..52459671hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38718
hg19718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434661
Supporting Variants
SamplesNB10
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15747014
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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