A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462935



Internal ID21120488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45365307..45369057hg38UCSC Ensembl
chr11:45386858..45390608hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg383751
hg193751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991702
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462935
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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