A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17396876



Internal ID22454746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96261534..96261534hg38UCSC Ensembl
chr1:96727090..96727090hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5950349
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17396876
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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