A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403849



Internal ID21061402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161566519..161664767hg38UCSC Ensembl
chr5:160993525..161091773hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3898249
hg1998249
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215944
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403849
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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