A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457135



Internal ID21114688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:62599296..62602103hg38UCSC Ensembl
chr12:62993076..62995883hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg382808
hg192808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002106
Samples
Known GenesC12orf61
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457135
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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