A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066514



Internal ID21457597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85277341..85277341hg38UCSC Ensembl
chr1:85743024..85743024hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5607802
Supporting Variants
SamplesHG02587
Known GenesLOC646626
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066514
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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