A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456060



Internal ID21113613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7322982..7338158hg38UCSC Ensembl
chr12:7475578..7490754hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3815177
hg1915177
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182532
Samples
Known GenesACSM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456060
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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