A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988229



Internal ID20555269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134036001..134038600hg38UCSC Ensembl
chr11:133905896..133908495hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471543
Supporting Variants
Samples
Known GenesLOC100128239
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988229
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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