A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580307



Internal ID21528796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65972197..65974137hg38UCSC Ensembl
chr5:65268025..65269965hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg381941
hg191941
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17149164
SamplesHG02011
Known GenesERBB2IP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580307
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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