A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449137



Internal ID21106690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2614401..2616000hg38UCSC Ensembl
chr11:2635631..2637230hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989577
Samples
Known GenesKCNQ1, KCNQ1OT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449137
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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