A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009256



Internal ID18751787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:844111..979954hg38UCSC Ensembl
Innerchr3:885794..1021638hg19UCSC Ensembl
Innerchr3:860794..996638hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38135844
hg19135845
hg18135845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590287
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)nsv1009256
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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