A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17403926



Internal ID22461796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206225736..206225736hg38UCSC Ensembl
chr2:207090460..207090460hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5959812
Supporting Variants
Samples
Known GenesGPR1-AS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17403926
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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