A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527096



Internal ID15107703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:151498616..151525837hg38UCSC Ensembl
Innerchr5:150878177..150905398hg19UCSC Ensembl
Innerchr5:150858370..150885591hg18UCSC Ensembl
Innerchr5:150858370..150885591hg17UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3827222
hg1927222
hg1827222
hg1727222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703475
Samples
Known GenesFAT2, MIR6499
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527096
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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