A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491142



Internal ID21148695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112014506..112016109hg38UCSC Ensembl
chr12:112452310..112453913hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg381604
hg191604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997000
Samples
Known GenesERP29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491142
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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