A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020584



Internal ID19109803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:31164391..31254118hg38UCSC Ensembl
Innerchr9:31164389..31254116hg19UCSC Ensembl
Innerchr9:31154389..31244116hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3889728
hg1989728
hg1889728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7509n100
Supporting Variantsnssv3688846
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)nsv1020584
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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