A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071613



Internal ID21436857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70554970..70554970hg38UCSC Ensembl
chr10:72314726..72314726hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38218
hg19218
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633026
Supporting Variants
SamplesHG00731
Known GenesPALD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071613
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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