A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988587



Internal ID20555627
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 StatusS
Merged Variantsnsv6471242
Supporting Variants
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988587
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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