A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485661



Internal ID21143214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124489008..124491760hg38UCSC Ensembl
chr12:124973554..124976306hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg382753
hg192753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997269
Samples
Known GenesNCOR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485661
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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