A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455595



Internal ID21113148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99290701..99291700hg38UCSC Ensembl
chr11:99161432..99162431hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996541
Samples
Known GenesCNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455595
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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