A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430488



Internal ID21088041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10813181..10819331hg38UCSC Ensembl
chr8:10670691..10676841hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg386151
hg196151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162175
Samples
Known GenesPINX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430488
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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