A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149971



Internal ID21476311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:66018447..66018599hg38UCSC Ensembl
chr5:65314275..65314427hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5566706
Supporting Variants
SamplesHG03486
Known GenesERBB2IP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149971
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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