A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614962



Internal ID16055685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101442332..101478426hg38UCSC Ensembl
Innerchr9:104204614..104240708hg19UCSC Ensembl
Innerchr9:103244435..103280529hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3836095
hg1936095
hg1836095
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1140221
Samples
Known GenesTMEM246
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614962
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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