A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527329



Internal ID15454622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8253580..8255151hg38UCSC Ensembl
Innerchr11:8275127..8276698hg19UCSC Ensembl
Innerchr11:8231703..8233274hg18UCSC Ensembl
Innerchr11:8231703..8233274hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381572
hg191572
hg181572
hg171572
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703754
Samples
Known GenesLMO1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527329
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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