A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052684



Internal ID18795215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105820663..105967999hg38UCSC Ensembl
Innerchr9:108582944..108730280hg19UCSC Ensembl
Innerchr9:107622765..107770101hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38147337
hg19147337
hg18147337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7698n100
Supporting Variantsnssv3697645
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)nsv1052684
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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