A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636101



Internal ID21828148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45749764..45749864hg38UCSC Ensembl
chr19:46253022..46253122hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6041696
Supporting Variants
Samples
Known GenesLOC388553
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636101
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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