A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447163



Internal ID21104716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16932373..17059004hg38UCSC Ensembl
chr11:16953920..17080551hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38126632
hg19126632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988738
Samples
Known GenesOR7E14P, PLEKHA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447163
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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