A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425841



Internal ID21083394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13024098..13072289hg38UCSC Ensembl
chr8:12881607..12929798hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3848192
hg1948192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165072
Samples
Known GenesKIAA1456
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425841
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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