A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465703



Internal ID21123256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44762051..44763330hg38UCSC Ensembl
chr11:44783601..44784880hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381280
hg191280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991705
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465703
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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