A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049137



Internal ID19138356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104203861..104371467hg38UCSC Ensembl
Innerchr9:106966142..107133748hg19UCSC Ensembl
Innerchr9:106005963..106173569hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38167607
hg19167607
hg18167607
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759801
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049137
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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