A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490244



Internal ID21147797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108569210..108573500hg38UCSC Ensembl
chr12:108962986..108967276hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg384291
hg194291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996216
Samples
Known GenesISCU
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490244
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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