A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465968



Internal ID21123521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:52689301..52694100hg38UCSC Ensembl
chr12:53083085..53087884hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188400
Samples
Known GenesKRT77
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465968
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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