A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008525



Internal ID18751056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4038501..4055218hg38UCSC Ensembl
Innerchr3:4080185..4096902hg19UCSC Ensembl
Innerchr3:4055185..4071902hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3816718
hg1916718
hg1816718
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590412
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)nsv1008525
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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