A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464507



Internal ID21122060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45000051..45001122hg38UCSC Ensembl
chr11:45021602..45022673hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381072
hg191072
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991680
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464507
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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