A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458963



Internal ID21116516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119543910..119676089hg38UCSC Ensembl
chr11:119414620..119546799hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38132180
hg19132180
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179467
Samples
Known GenesPVRL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458963
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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