A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008570



Internal ID18751101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4125592..4271801hg38UCSC Ensembl
Innerchr3:4167276..4313485hg19UCSC Ensembl
Innerchr3:4142276..4288485hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38146210
hg19146210
hg18146210
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4652n100
Supporting Variantsnssv3590484, nssv3739577, nssv3590483
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)nsv1008570
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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