A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17142299



Internal ID21454165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74886656..74891227hg38UCSC Ensembl
chr5:74182481..74187052hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg384572
hg194572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580247
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17142299
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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