A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465749



Internal ID21123302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66002401..66003000hg38UCSC Ensembl
chr11:65769872..65770471hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992536
Samples
Known GenesBANF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465749
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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