A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039904



Internal ID19129123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:40834692..40987414hg38UCSC Ensembl
Innerchr11:40856242..41008964hg19UCSC Ensembl
Innerchr11:40812818..40965540hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38152723
hg19152723
hg18152723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3509666
Samples
Known GenesLRRC4C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039904
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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