A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464818



Internal ID21122371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132053201..132074600hg38UCSC Ensembl
chr11:131923095..131944494hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3821400
hg1921400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1340n223
Supporting Variantsnssv17988557
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464818
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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