A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449646



Internal ID21107199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16793016..16796416hg38UCSC Ensembl
chr11:16814563..16817963hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg383401
hg193401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988535
Samples
Known GenesPLEKHA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449646
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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