A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462986



Internal ID21120539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31995545..31997593hg38UCSC Ensembl
chr12:32148479..32150527hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg382049
hg192049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000728
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462986
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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