A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413695



Internal ID21071248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53648901..53657700hg38UCSC Ensembl
chr6:53513699..53522498hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg388800
hg198800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224946
Samples
Known GenesKLHL31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413695
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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