A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17099264



Internal ID21445062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:71291308..71291377hg38UCSC Ensembl
chr13:71865440..71865509hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586676
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17099264
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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