A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086448



Internal ID21479872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40220591..40220591hg38UCSC Ensembl
chr17:38376843..38376843hg19UCSC Ensembl
Cytoband17q21.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661756
Supporting Variants
SamplesHG03683
Known GenesWIPF2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086448
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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