A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071599



Internal ID21505638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70206855..70206855hg38UCSC Ensembl
chr10:71966611..71966611hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5626708
Supporting Variants
SamplesNA19650
Known GenesPPA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071599
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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