A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361932



Internal ID21019485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11515927..11543404hg38UCSC Ensembl
chr4:11517551..11545028hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3827478
hg1927478
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210177
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361932
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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