A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434395



Internal ID21091948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13160826..13162680hg38UCSC Ensembl
chr8:13018335..13020189hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381855
hg191855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165637
Samples
Known GenesDLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434395
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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