A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3506289



Internal ID18457884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:97226625..97287718hg38UCSC Ensembl
Innerchr10:98986382..99047475hg19UCSC Ensembl
Innerchr10:98976372..99037465hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3861094
hg1961094
hg1861094
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040903
Supporting Variants
Samples
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3506289
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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