A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354110



Internal ID21011663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:78452808..78618801hg38UCSC Ensembl
chr2:78679934..78845927hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38165994
hg19165994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18091387
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354110
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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