A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024541



Internal ID19113758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:31560620..31603347hg38UCSC Ensembl
Innerchr9:31560618..31603345hg19UCSC Ensembl
Innerchr9:31550618..31593345hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3842728
hg1942728
hg1842728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7513n100
Supporting Variantsnssv3688855
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)nsv1024541
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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