A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412441



Internal ID21069994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42715286..42720603hg38UCSC Ensembl
chr6:42683024..42688341hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg385318
hg195318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143384
Samples
Known GenesPRPH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412441
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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