A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17156455



Internal ID21459661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79270573..79270624hg38UCSC Ensembl
chr5:78566396..78566447hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5576137
Supporting Variants
SamplesHG02818
Known GenesJMY
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17156455
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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