A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465614



Internal ID21123167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10470174..10478750hg38UCSC Ensembl
chr12:10622773..10631349hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg388577
hg198577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995924
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465614
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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