A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030568



Internal ID19119787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4903296..4948105hg38UCSC Ensembl
Innerchr9:4903296..4948105hg19UCSC Ensembl
Innerchr9:4893296..4938105hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3844810
hg1944810
hg1844810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7381n100
Supporting Variantsnssv3758095
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)nsv1030568
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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