A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462991



Internal ID21120544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51525232..51542909hg38UCSC Ensembl
chr12:51919016..51936693hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3817678
hg1917678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002157
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462991
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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