A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430750



Internal ID21088303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38521344..38549975hg38UCSC Ensembl
chr8:38378862..38407493hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3828632
hg1928632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168964
Samples
Known GenesC8orf86
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430750
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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