A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17369630



Internal ID22595299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154607872..154607872hg38UCSC Ensembl
chr1:154580348..154580348hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38218
hg19218
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5952515
Supporting Variants
Samples
Known GenesADAR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17369630
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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