A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071201



Internal ID21451013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:60235910..60235910hg38UCSC Ensembl
chr10:61995668..61995668hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633421
Supporting Variants
SamplesHG01505
Known GenesANK3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071201
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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