A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384948



Internal ID21042501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112218401..112236100hg38UCSC Ensembl
chr4:113139557..113157256hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3817700
hg1917700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5417n223
Supporting Variantsnssv18209541
Samples
Known GenesAP1AR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384948
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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