A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049535



Internal ID19138754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:21362586..21432920hg38UCSC Ensembl
Innerchr11:21384132..21454466hg19UCSC Ensembl
Innerchr11:21340708..21411042hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3870335
hg1970335
hg1870335
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3511993
Samples
Known GenesNELL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049535
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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