A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710115



Internal ID19008396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:40328053..40455244hg38UCSC Ensembl
Innerchr11:40349603..40476794hg19UCSC Ensembl
Innerchr11:40306179..40433370hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38127192
hg19127192
hg18127192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054514
Supporting Variants
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)nssv3710115
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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