A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035315



Internal ID19124534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112234047..112309365hg38UCSC Ensembl
Innerchr9:114996327..115071645hg19UCSC Ensembl
Innerchr9:114036148..114111466hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3875319
hg1975319
hg1875319
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695052
Samples
Known GenesMIR3134, PTBP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035315
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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