A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050280



Internal ID19139499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76519062..76545535hg38UCSC Ensembl
Innerchr9:79133978..79160451hg19UCSC Ensembl
Innerchr9:78323798..78350271hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3826474
hg1926474
hg1826474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3696365, nssv3696367, nssv3696366
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)nsv1050280
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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