A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv747289



Internal ID16041245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42257742..42443698hg38UCSC Ensembl
Innerchr10:42753190..42939146hg19UCSC Ensembl
Innerchr10:42073196..42259152hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg38185957
hg19185957
hg18185957
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550671
Supporting Variants
Samples
Known GenesCCNYL2, LOC441666
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv747289
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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