A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037066



Internal ID19126285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:40662049..40761741hg38UCSC Ensembl
Innerchr11:40683599..40783291hg19UCSC Ensembl
Innerchr11:40640175..40739867hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3899693
hg1999693
hg1899693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504556, nssv3522133
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)nsv1037066
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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