A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016281



Internal ID19105500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19842237..19990274hg38UCSC Ensembl
Innerchr9:19842235..19990272hg19UCSC Ensembl
Innerchr9:19832235..19980272hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38148038
hg19148038
hg18148038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755829
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)nsv1016281
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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