A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463976



Internal ID21121529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:15891799..15955106hg38UCSC Ensembl
chr12:16044733..16108040hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3863308
hg1963308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997656
Samples
Known GenesDERA, STRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463976
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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