A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463629



Internal ID21121182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98451968..98476364hg38UCSC Ensembl
chr12:98845746..98870142hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3824397
hg1924397
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190687
Samples
Known GenesSLC9A7P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463629
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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