A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003471



Internal ID19092689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164258447..164376855hg38UCSC Ensembl
Innerchr3:163976235..164094643hg19UCSC Ensembl
Innerchr3:165458929..165577337hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38118409
hg19118409
hg18118409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4969n100
Supporting Variantsnssv3614539
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)nsv1003471
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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