A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv747365



Internal ID15694635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46526513..46708317hg38UCSC Ensembl
Innerchr10:46841300..47028331hg19UCSC Ensembl
Innerchr10:46261306..46448337hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38181805
hg19187032
hg18187032
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550722
Supporting Variants
Samples
Known GenesFAM35BP, GPRIN2, SYT15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv747365
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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