A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696351



Internal ID18994632
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 StatusS
Merged Variantsnsv1043383
Supporting Variants
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)nssv3696351
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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