A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001174



Internal ID19090391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:193217628..193394242hg38UCSC Ensembl
Innerchr1:193186758..193363372hg19UCSC Ensembl
Innerchr1:191453381..191629995hg18UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg38176615
hg19176615
hg18176615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3484353
Samples
Known GenesCDC73
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001174
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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