A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035734



Internal ID18778265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103712908..103965576hg38UCSC Ensembl
Innerchr9:106475190..106727857hg19UCSC Ensembl
Innerchr9:105515011..105767678hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38252669
hg19252668
hg18252668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697614, nssv3697615
Samples
Known GenesMIR6130
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035734
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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