A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021605



Internal ID18764139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:18002207..18271111hg38UCSC Ensembl
Innerchr9:18002205..18271109hg19UCSC Ensembl
Innerchr9:17992205..18261109hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38268905
hg19268905
hg18268905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755826
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)nsv1021605
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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