A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987937



Internal ID20554977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131705601..131706900hg38UCSC Ensembl
chr11:131575495..131576794hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462966
Supporting Variants
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987937
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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