A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527734



Internal ID15455027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:123572667..123585409hg38UCSC Ensembl
Innerchr5:122908361..122921103hg19UCSC Ensembl
Innerchr5:122936260..122949002hg18UCSC Ensembl
Innerchr5:122936260..122949002hg17UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3812743
hg1912743
hg1812743
hg1712743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704218
Samples
Known GenesCSNK1G3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527734
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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