A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv840703



Internal ID15787973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:37080410..37460700hg38UCSC Ensembl
Innerchr15:37372611..37752901hg19UCSC Ensembl
Innerchr15:35159903..35540193hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38380291
hg19380291
hg18380291
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569200
Supporting Variants
Samples
Known GenesMEIS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv840703
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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