A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444672



Internal ID21102225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16865934..16873760hg38UCSC Ensembl
chr11:16887481..16895307hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg387827
hg197827
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181270
Samples
Known GenesPLEKHA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444672
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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