A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024128



Internal ID19113345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:157628595..157640707hg38UCSC Ensembl
Innerchr4:158549747..158561859hg19UCSC Ensembl
Innerchr4:158769197..158781309hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3812113
hg1912113
hg1812113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5446n100
Supporting Variantsnssv3636151, nssv3636149, nssv3636150
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)nsv1024128
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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