A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081064



Internal ID21467268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40900680..40900806hg38UCSC Ensembl
chr13:41474816..41474942hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590749
Supporting Variants
SamplesHG03065
Known GenesTPTE2P5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081064
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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