A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017523



Internal ID19106740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24930303..25019895hg38UCSC Ensembl
Innerchr9:24930301..25019893hg19UCSC Ensembl
Innerchr9:24920301..25009893hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3889593
hg1989593
hg1889593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7482n100
Supporting Variantsnssv3690851
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)nsv1017523
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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