A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031559



Internal ID19120781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:179735578..179824530hg38UCSC Ensembl
Innerchr4:180656731..180745683hg19UCSC Ensembl
Innerchr4:180893725..180982677hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3888953
hg1988953
hg1888953
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3744528
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)nsv1031559
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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