A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319678



Internal ID20852773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9074063..9076871hg38UCSC Ensembl
chr1:9134122..9136930hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg382809
hg192809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065089
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319678
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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