A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032702



Internal ID19121924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13723813..13760987hg38UCSC Ensembl
Innerchr9:13723812..13760986hg19UCSC Ensembl
Innerchr9:13713812..13750986hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3837175
hg1937175
hg1837175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690614
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)nsv1032702
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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