A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662334



Internal ID21610639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37712436..37712436hg38UCSC Ensembl
chr17:36072444..36072444hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17097421
SamplesNA19983
Known GenesHNF1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662334
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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