A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366311



Internal ID21023864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3426615..4165741hg38UCSC Ensembl
chr4:3428342..4167468hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38739127
hg19739127
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212917
Samples
Known GenesADRA2C, DOK7, FAM86EP, HGFAC, LINC00955, LOC100133461, LRPAP1, RGS12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366311
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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