A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042965



Internal ID19132184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:107338464..107364380hg38UCSC Ensembl
Innerchr9:110100745..110126661hg19UCSC Ensembl
Innerchr9:109140566..109166482hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3825917
hg1925917
hg1825917
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697647
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)nsv1042965
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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