A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458734



Internal ID21116287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45018501..45019200hg38UCSC Ensembl
chr12:45412284..45412983hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000379
Samples
Known GenesDBX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458734
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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