A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434661



Internal ID21396663
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 StatusM
Merged Variantsdgv640n172
Supporting Variantsnssv15747014, nssv15750562
SamplesNB10, SMI018
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434661
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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