A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467652



Internal ID21125205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30596987..30606965hg38UCSC Ensembl
chr12:30749921..30759899hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg389979
hg199979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998943
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467652
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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