A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17595344



Internal ID21787387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97262029..97269143hg38UCSC Ensembl
chr10:99021786..99028900hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg387115
hg197115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005603
Supporting Variants
Samples
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17595344
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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