A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463535



Internal ID21121088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:105336278..105340410hg38UCSC Ensembl
chr12:105730056..105734188hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg384133
hg194133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995964
Samples
Known GenesC12orf75
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463535
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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