A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017904



Internal ID19107121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:147892982..148054197hg38UCSC Ensembl
Innerchr4:148814133..148975348hg19UCSC Ensembl
Innerchr4:149033583..149194798hg18UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38161216
hg19161216
hg18161216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636069
Samples
Known GenesARHGAP10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017904
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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