A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434126



Internal ID21396128
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 StatusM
Merged Variantsdgv551n172
Supporting Variantsnssv15753837, nssv15749076, nssv15753448, nssv15749188, nssv15746674, nssv15751279, nssv15748647, nssv15747633, nssv15753191, nssv15754343
SamplesNB12, SMI034, NB08, NB10, BTQ016, SMI041, NB11, NB07, SMI018, NB09
Known GenesZNF595, ZNF718
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434126
Frequency
Sample Size15
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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