A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432234



Internal ID21089787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30301272..30313971hg38UCSC Ensembl
chr8:30158788..30171487hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3812700
hg1912700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166844
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432234
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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