A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034518



Internal ID19123740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:18166901..18214880hg38UCSC Ensembl
Innerchr9:18166899..18214878hg19UCSC Ensembl
Innerchr9:18156899..18204878hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3847980
hg1947980
hg1847980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690673
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)nsv1034518
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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