A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470491



Internal ID21128044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:97357101..97359800hg38UCSC Ensembl
chr12:97750879..97753578hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006037
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470491
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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