A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527861



Internal ID15108468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15848363..16941367hg38UCSC Ensembl
Innerchr4:15849986..16942990hg19UCSC Ensembl
Innerchr4:15459084..16552088hg18UCSC Ensembl
Innerchr4:15526255..16619259hg17UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg381093005
hg191093005
hg181093005
hg171093005
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704359
Samples
Known GenesCD38, FGFBP1, FGFBP2, LDB2, MIR548AX, PROM1, TAPT1, TAPT1-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527861
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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