A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17134063



Internal ID21453597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149111732..149111781hg38UCSC Ensembl
chr5:148491295..148491344hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570283
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17134063
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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