A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413544



Internal ID21071097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35750965..35760001hg38UCSC Ensembl
chr6:35718742..35727778hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg389037
hg199037
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234480
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413544
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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