A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17111873



Internal ID21424276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:233176499..233176499hg38UCSC Ensembl
chr2:234085145..234085145hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38648
hg19648
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5607344
Supporting Variants
SamplesHG00731
Known GenesINPP5D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17111873
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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