A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17529199



Internal ID21853556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:236416727..236416727hg38UCSC Ensembl
chr2:237325370..237325370hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6053115
Supporting Variants
Samples
Known GenesIQCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17529199
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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