A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028901



Internal ID19118120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19993848..20061896hg38UCSC Ensembl
Innerchr9:19993846..20061894hg19UCSC Ensembl
Innerchr9:19983846..20051894hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3868049
hg1968049
hg1868049
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7471n100
Supporting Variantsnssv3690694
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)nsv1028901
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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