A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464874



Internal ID21122427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:49323206..49327915hg38UCSC Ensembl
chr12:49716989..49721698hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg384710
hg194710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001949
Samples
Known GenesTROAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464874
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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