A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018593



Internal ID19107810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:22418953..22479006hg38UCSC Ensembl
Innerchr6:22419182..22479235hg19UCSC Ensembl
Innerchr6:22527161..22587214hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3860054
hg1960054
hg1860054
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654830
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)nsv1018593
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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