A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412582



Internal ID21070135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63346927..63359567hg38UCSC Ensembl
chr6:64056832..64069472hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3812641
hg1912641
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223802
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412582
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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