A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv746945



Internal ID16040901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38576045..38677569hg38UCSC Ensembl
Innerchr10:38869176..38970700hg19UCSC Ensembl
Innerchr10:38909182..39010706hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38101525
hg19101525
hg18101525
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550474
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv746945
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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