A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014219



Internal ID18756753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:8577052..8722805hg38UCSC Ensembl
Innerchr4:8578779..8724531hg19UCSC Ensembl
Innerchr4:8629679..8775431hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38145754
hg19145753
hg18145753
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3738145
Samples
Known GenesCPZ, GPR78
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014219
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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