A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995437



Internal ID20562477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96033101..96036600hg38UCSC Ensembl
chr11:95766265..95769764hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470930
Supporting Variants
Samples
Known GenesMAML2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995437
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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