A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016576



Internal ID19105795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:175077424..175318559hg38UCSC Ensembl
Innerchr4:175998575..176239710hg19UCSC Ensembl
Innerchr4:176235150..176476705hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38241136
hg19241136
hg18241556
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3744521
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016576
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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