A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030848



Internal ID19120067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:1466368..1675561hg38UCSC Ensembl
Innerchr9:1466368..1675561hg19UCSC Ensembl
Innerchr9:1456368..1665561hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38209194
hg19209194
hg18209194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691231
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)nsv1030848
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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