A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045225



Internal ID19134444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:103330217..103583931hg38UCSC Ensembl
Innerchr11:103200945..103454659hg19UCSC Ensembl
Innerchr11:102706155..102959869hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38253715
hg19253715
hg18253715
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508050
Samples
Known GenesDYNC2H1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045225
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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