A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458546



Internal ID21116099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:5818174..5826409hg38UCSC Ensembl
chr12:5927340..5935575hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg388236
hg198236
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193958
Samples
Known GenesANO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458546
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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