A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472835



Internal ID21130388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102930631..102940963hg38UCSC Ensembl
chr12:103324409..103334741hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg3810333
hg1910333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995614
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472835
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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