A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018321



Internal ID19107538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:1444746..1556848hg38UCSC Ensembl
Innerchr9:1444746..1556848hg19UCSC Ensembl
Innerchr9:1434746..1546848hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38112103
hg19112103
hg18112103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691230, nssv3691228, nssv3691229
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)nsv1018321
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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