A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022133



Internal ID19111351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64683555..64913310hg38UCSC Ensembl
Innerchr9:69695973..69925728hg19UCSC Ensembl
Innerchr9:68985793..69215548hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38229756
hg19229756
hg18229756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7660n100
Supporting Variantsnssv3696161, nssv3696162
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)nsv1022133
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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