A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032178



Internal ID19121400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185915475..185988442hg38UCSC Ensembl
Innerchr4:186836629..186909596hg19UCSC Ensembl
Innerchr4:187073623..187146590hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3872968
hg1972968
hg1872968
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635628
Samples
Known GenesSORBS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032178
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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