A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15747633



Internal ID21390180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10001..69108hg38UCSC Ensembl
chr4:10001..69000hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3859108
hg1959000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434126
Supporting Variants
SamplesNB10
Known GenesZNF595, ZNF718
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15747633
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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