A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035575



Internal ID18778106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7648656..7744807hg38UCSC Ensembl
Innerchr11:7669887..7766354hg19UCSC Ensembl
Innerchr11:7626463..7722930hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3896152
hg1996468
hg1896468
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3708511
Samples
Known GenesCYB5R2, OVCH2, PPFIBP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035575
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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