A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17407897



Internal ID22465767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:172657429..172657429hg38UCSC Ensembl
chr2:173522157..173522157hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5948513
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17407897
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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