A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068566



Internal ID21435628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118423950..118423950hg38UCSC Ensembl
chr10:120183462..120183462hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg384163
hg194163
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5643358
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068566
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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