A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469531



Internal ID21127084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:77128140..77134124hg38UCSC Ensembl
chr12:77521920..77527904hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg385985
hg195985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004144
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469531
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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