A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025884



Internal ID19115101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29838954..29875105hg38UCSC Ensembl
Innerchr9:29838952..29875103hg19UCSC Ensembl
Innerchr9:29828952..29865103hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3836152
hg1936152
hg1836152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688777
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)nsv1025884
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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