A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470292



Internal ID21127845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:21836226..21836902hg38UCSC Ensembl
chr12:21989160..21989836hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998228
Samples
Known GenesABCC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470292
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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