A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156243



Internal ID22086748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152069134..152071589hg38UCSC Ensembl
Outerchr4:152068448..152072978hg38UCSC Ensembl
Innerchr4:152990286..152992741hg19UCSC Ensembl
Outerchr4:152989600..152994130hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg384531
hg194531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015693, nssv4015689, nssv4015703, nssv4015686, nssv4015699, nssv4015690, nssv4015708, nssv4015695, nssv4015706, nssv4015687, nssv4015701, nssv4015696, nssv4015704, nssv4015685, nssv4015694, nssv4015697, nssv4015691, nssv4015705, nssv4015692, nssv4015702, nssv4015698, nssv4015688, nssv4015700, nssv4015707
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156243
Frequency
Sample Size131
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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