A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427397



Internal ID21084950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58210673..58262220hg38UCSC Ensembl
chr8:59123232..59174779hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3851548
hg1951548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169954
Samples
Known GenesLOC101929528
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427397
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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