A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415749



Internal ID21073302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34334330..34334825hg38UCSC Ensembl
chr8:34191848..34192343hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166701
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415749
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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