A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3505822



Internal ID18804103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:40385971..40500169hg38UCSC Ensembl
Innerchr11:40407521..40521719hg19UCSC Ensembl
Innerchr11:40364097..40478295hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38114199
hg19114199
hg18114199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039332
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)nssv3505822
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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