A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026158



Internal ID19115375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:154076513..154126379hg38UCSC Ensembl
Innerchr4:154997665..155047531hg19UCSC Ensembl
Innerchr4:155217115..155266981hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3849867
hg1949867
hg1849867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636130, nssv3636129
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)nsv1026158
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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