A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430996



Internal ID21088549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:107260811..107262375hg38UCSC Ensembl
chr8:108273039..108274603hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg381565
hg191565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162090
Samples
Known GenesANGPT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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