A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462431



Internal ID21119984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:39465355..39466594hg38UCSC Ensembl
chr12:39859157..39860396hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180425
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462431
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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