A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458753



Internal ID21116306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:52788646..52790390hg38UCSC Ensembl
chr12:53182430..53184174hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg381745
hg191745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001408
Samples
Known GenesKRT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458753
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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