A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328080



Internal ID20861225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8161363..8171064hg38UCSC Ensembl
chr1:8221423..8231124hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg389702
hg199702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064448
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328080
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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