A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393072



Internal ID21050625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:127105797..127119060hg38UCSC Ensembl
chr4:128026952..128040215hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg3813264
hg1913264
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210289
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393072
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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