A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003562



Internal ID19092780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:43029418..43088544hg38UCSC Ensembl
Innerchr4:43031435..43090561hg19UCSC Ensembl
Innerchr4:42726192..42785318hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3859127
hg1959127
hg1859127
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739362
Samples
Known GenesGRXCR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003562
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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