A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447638



Internal ID21105191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22789381..22793253hg38UCSC Ensembl
chr11:22810927..22814799hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg383873
hg193873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988772
Samples
Known GenesGAS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447638
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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