A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459924



Internal ID21117477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:76711823..76720279hg38UCSC Ensembl
chr12:77105603..77114059hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg388457
hg198457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004117
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459924
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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