A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040072



Internal ID19129291
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 StatusM
Merged Variants
Supporting Variantsnssv3511727
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)nsv1040072
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer