A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473939



Internal ID21131492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118540862..118543999hg38UCSC Ensembl
chr11:118411577..118414714hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383138
hg193138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987197
Samples
Known GenesTMEM25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473939
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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