A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090080



Internal ID21432805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37607838..37607838hg38UCSC Ensembl
chr13:38181975..38181975hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649156
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090080
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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