A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461831



Internal ID21119384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99610595..99682149hg38UCSC Ensembl
chr11:99481326..99552880hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3871555
hg1971555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996581
Samples
Known GenesCNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461831
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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