A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067164



Internal ID21490937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:95005419..95005419hg38UCSC Ensembl
chr1:95470975..95470975hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5616116
Supporting Variants
SamplesNA19238
Known GenesALG14
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067164
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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