A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434127



Internal ID21396129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10001..70108hg38UCSC Ensembl
chr4:10001..70000hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3860108
hg1960000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv551n172
Supporting Variantsnssv15750683, nssv15745995, nssv15746779, nssv15747211, nssv15751455
SamplesMDQ045, BTQ038, BTQ055, MDQ010, MDQ025
Known GenesZNF595, ZNF718
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434127
Frequency
Sample Size15
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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