A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15178099



Internal ID21316895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37126244..37126293hg38UCSC Ensembl
chr20:35754647..35754696hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3945313
Supporting Variants
SamplesHG002
Known GenesMROH8
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15178099
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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