A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471242



Internal ID21128795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132241120..132241826hg38UCSC Ensembl
chr11:132111014..132111720hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988587
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471242
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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