A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033655



Internal ID19122876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22509329..22565474hg38UCSC Ensembl
Innerchr9:22509328..22565473hg19UCSC Ensembl
Innerchr9:22499328..22555473hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3856146
hg1956146
hg1856146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690727, nssv3690726
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)nsv1033655
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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