A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067656



Internal ID21446829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126121102..126121102hg38UCSC Ensembl
chr10:127809671..127809671hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634009
Supporting Variants
SamplesHG00732
Known GenesADAM12
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067656
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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