A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067649



Internal ID21479039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125731795..125731795hg38UCSC Ensembl
chr10:127420364..127420364hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382336
hg192336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5636388
Supporting Variants
SamplesHG03486
Known GenesC10orf137
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067649
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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