A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491228



Internal ID21148781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95252452..95274918hg38UCSC Ensembl
chr13:95904706..95927172hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3822467
hg1922467
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187086
Samples
Known GenesABCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491228
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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