A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343023



Internal ID21000576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:86860901..86865600hg38UCSC Ensembl
chr2:87088024..87092723hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18091780
Samples
Known GenesANAPC1P1, CD8B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343023
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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