A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015235



Internal ID19104452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13308617..13340591hg38UCSC Ensembl
Innerchr9:13308616..13340590hg19UCSC Ensembl
Innerchr9:13298616..13330590hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3831975
hg1931975
hg1831975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7458n100
Supporting Variantsnssv3690610, nssv3690609
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)nsv1015235
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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