A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463505



Internal ID21121058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:74607001..74625900hg38UCSC Ensembl
chr12:75000781..75019680hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg3818900
hg1918900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1610n223
Supporting Variantsnssv18003476
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463505
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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