A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437646



Internal ID21095199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22818812..22829324hg38UCSC Ensembl
chr11:22840358..22850870hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3810513
hg1910513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988776
Samples
Known GenesSVIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437646
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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