A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093059



Internal ID21456411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95196582..95196582hg38UCSC Ensembl
chr13:95848836..95848836hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649060
Supporting Variants
SamplesHG02492
Known GenesABCC4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093059
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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