A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511727



Internal ID18810008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:40379322..40572682hg38UCSC Ensembl
Innerchr11:40400872..40594232hg19UCSC Ensembl
Innerchr11:40357448..40550808hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38193361
hg19193361
hg18193361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040072
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)nssv3511727
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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