A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466007



Internal ID21123560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:39689096..39689439hg38UCSC Ensembl
chr12:40082898..40083241hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000357
Samples
Known GenesC12orf40
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466007
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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