A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031815



Internal ID19121037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:148251333..148361776hg38UCSC Ensembl
Innerchr4:149172485..149282928hg19UCSC Ensembl
Innerchr4:149391935..149502378hg18UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38110444
hg19110444
hg18110444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636071
Samples
Known GenesNR3C2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031815
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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