A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475392



Internal ID21132945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:72208961..72209536hg38UCSC Ensembl
chr12:72602741..72603316hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002950
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475392
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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