A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382607



Internal ID21040160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163326801..163355000hg38UCSC Ensembl
chr4:164247953..164276152hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3828200
hg1928200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5543n223
Supporting Variantsnssv18213755
Samples
Known GenesNPY1R, NPY5R
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382607
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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