A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020616



Internal ID19109835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30419932..30565062hg38UCSC Ensembl
Innerchr9:30419930..30565060hg19UCSC Ensembl
Innerchr9:30409930..30555060hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38145131
hg19145131
hg18145131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7504n100
Supporting Variantsnssv3688824, nssv3688825, nssv3688823
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)nsv1020616
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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