A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421900



Internal ID21079453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65179101..65181600hg38UCSC Ensembl
chr8:66091336..66093835hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169339
Samples
Known GenesLINC00251
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421900
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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