A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403244



Internal ID21060797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42894395..42903340hg38UCSC Ensembl
chr6:42862133..42871078hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg388946
hg198946
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217204
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403244
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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