A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031451



Internal ID19120673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:31172352..31599616hg38UCSC Ensembl
Innerchr9:31172350..31599614hg19UCSC Ensembl
Innerchr9:31162350..31589614hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38427265
hg19427265
hg18427265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7510n100
Supporting Variantsnssv3755925
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)nsv1031451
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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