A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434588



Internal ID21396590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178729883..178731798hg38UCSC Ensembl
chr5:178156884..178158799hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg381916
hg191916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15749642
SamplesMDQ025
Known GenesZNF354A
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434588
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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