A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043383



Internal ID19132602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:70902146..70941763hg38UCSC Ensembl
Innerchr9:73517062..73556679hg19UCSC Ensembl
Innerchr9:72706882..72746499hg18UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3839618
hg1939618
hg1839618
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3696351
Samples
Known GenesTRPM3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043383
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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