A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492955



Internal ID21150508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124931547..124942567hg38UCSC Ensembl
chr12:125416093..125427113hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3811021
hg1911021
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997301
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492955
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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