A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457311



Internal ID21114864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101573151..101577404hg38UCSC Ensembl
chr12:101966929..101971182hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg384254
hg194254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996702
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457311
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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