A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424147



Internal ID21081700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:131858389..131858974hg38UCSC Ensembl
chr8:132870636..132871221hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38586
hg19586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165653
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424147
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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