A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131234



Internal ID21495145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168704195..168704340hg38UCSC Ensembl
chr5:168131200..168131345hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582061
Supporting Variants
SamplesNA19238
Known GenesSLIT3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131234
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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