A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435050



Internal ID21092603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94933576..94933882hg38UCSC Ensembl
chr8:95945804..95946110hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171835
Samples
Known GenesTP53INP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435050
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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