A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472445



Internal ID21129998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72932350..72956902hg38UCSC Ensembl
chr11:72643395..72667947hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3824553
hg1924553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992808
Samples
Known GenesFCHSD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472445
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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