A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140973



Internal ID21454781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:66018446..66018506hg38UCSC Ensembl
chr5:65314274..65314334hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572058
Supporting Variants
SamplesHG02011
Known GenesERBB2IP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140973
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer