A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17126717



Internal ID21472947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151059802..151059853hg38UCSC Ensembl
chr5:150439363..150439414hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572948
Supporting Variants
SamplesHG03371
Known GenesTNIP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17126717
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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