A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474791



Internal ID21132344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:73913101..74031300hg38UCSC Ensembl
chr12:74306881..74425080hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38118200
hg19118200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18003437
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474791
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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