A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038630



Internal ID18781161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:22024274..22450043hg38UCSC Ensembl
Innerchr11:22045820..22471589hg19UCSC Ensembl
Innerchr11:22002396..22428165hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38425770
hg19425770
hg18425770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3510288
Samples
Known GenesANO5, SLC17A6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038630
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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