A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017524



Internal ID18760058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:176114932..176227598hg38UCSC Ensembl
Innerchr4:177036083..177148749hg19UCSC Ensembl
Innerchr4:177273077..177385743hg18UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg38112667
hg19112667
hg18112667
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635457
Samples
Known GenesASB5, MIR1267, SPATA4, WDR17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017524
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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