A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988558



Internal ID20555598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132054301..132078400hg38UCSC Ensembl
chr11:131924195..131948294hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3824100
hg1924100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6469747
Supporting Variants
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988558
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00025


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