A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033954



Internal ID20600994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9555541..9646884hg38UCSC Ensembl
chr16:9649398..9740741hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3891344
hg1991344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502950
Supporting Variants
Samples
Known GenesMIR7641-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033954
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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