A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3513857



Internal ID18465452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49126191..49427222hg38UCSC Ensembl
Innerchr11:49147743..49448774hg19UCSC Ensembl
Innerchr11:49104319..49405350hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38301032
hg19301032
hg18301032
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044070
Supporting Variants
Samples
Known GenesFOLH1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3513857
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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