A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431159



Internal ID21088712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:15217301..16863300hg38UCSC Ensembl
chr8:15074810..16720809hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381646000
hg191646000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7281n223
Supporting Variantsnssv18165195
Samples
Known GenesMSR1, SGCZ, TUSC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431159
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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