A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088056



Internal ID21473432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5197851..5197851hg38UCSC Ensembl
chr17:5101146..5101146hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654144
Supporting Variants
SamplesHG03371
Known GenesLOC100130950
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088056
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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