A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526075



Internal ID15453368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:88592636..88604997hg38UCSC Ensembl
Innerchr11:88325804..88338165hg19UCSC Ensembl
Innerchr11:87965452..87977813hg18UCSC Ensembl
Innerchr11:87965452..87977813hg17UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3812362
hg1912362
hg1812362
hg1712362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702316
Samples
Known GenesGRM5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526075
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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