A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527298



Internal ID8421573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2621030..2631092hg38UCSC Ensembl
Innerchr9:2621030..2631092hg19UCSC Ensembl
Innerchr9:2611030..2621092hg18UCSC Ensembl
Innerchr9:2611030..2621092hg17UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3810063
hg1910063
hg1810063
hg1710063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703716
Samples
Known GenesFLJ35024, VLDLR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527298
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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