A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588921



Internal ID21780964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97251786..97251786hg38UCSC Ensembl
chr10:99011543..99011543hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38551
hg19551
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6098239
Supporting Variants
Samples
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588921
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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