A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467956



Internal ID21125509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:103312172..103312560hg38UCSC Ensembl
chr12:103705950..103706338hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995635
Samples
Known GenesC12orf42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467956
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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