A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437637



Internal ID21095190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30053053..30073821hg38UCSC Ensembl
chr11:30074600..30095368hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3820769
hg1920769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990294
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437637
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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