A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467553



Internal ID21125106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:74609101..74623100hg38UCSC Ensembl
chr12:75002881..75016880hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg3814000
hg1914000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1611n223
Supporting Variantsnssv18003480
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467553
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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