A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471571



Internal ID21129124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73919354..73919889hg38UCSC Ensembl
chr11:73630399..73630934hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993887
Samples
Known GenesPAAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471571
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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