A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315841



Internal ID20848915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:79051377..79168527hg38UCSC Ensembl
chr1:79517062..79634212hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38117151
hg19117151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064226
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315841
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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