A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020675



Internal ID18763210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:32323273..32391249hg38UCSC Ensembl
Innerchr9:32323271..32391247hg19UCSC Ensembl
Innerchr9:32313271..32381247hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3867977
hg1967977
hg1867977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688865
Samples
Known GenesACO1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020675
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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