A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038637



Internal ID19127856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103958926..103987587hg38UCSC Ensembl
Innerchr9:106721207..106749868hg19UCSC Ensembl
Innerchr9:105761028..105789689hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3828662
hg1928662
hg1828662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697616
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)nsv1038637
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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