A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404392



Internal ID21061945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:49743567..49744077hg38UCSC Ensembl
chr6:49711280..49711790hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38511
hg19511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142823
Samples
Known GenesCRISP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404392
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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