A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462334



Internal ID21119887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:52167511..52183380hg38UCSC Ensembl
chr12:52561295..52577164hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3815870
hg1915870
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178097
Samples
Known GenesKRT80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462334
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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