A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023399



Internal ID19112616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30419932..30564599hg38UCSC Ensembl
Innerchr9:30419930..30564597hg19UCSC Ensembl
Innerchr9:30409930..30554597hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38144668
hg19144668
hg18144668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7504n100
Supporting Variantsnssv3688820, nssv3755918, nssv3755919, nssv3688819, nssv3688821
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)nsv1023399
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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