A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023270



Internal ID18765802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:154225348..154311669hg38UCSC Ensembl
Innerchr4:155146500..155232821hg19UCSC Ensembl
Innerchr4:155365950..155452271hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3886322
hg1986322
hg1886322
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636131
Samples
Known GenesDCHS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023270
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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