A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014326



Internal ID19103547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:158902760..158938025hg38UCSC Ensembl
Innerchr3:158620549..158655814hg19UCSC Ensembl
Innerchr3:160103243..160138508hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3835266
hg1935266
hg1835266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606400
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)nsv1014326
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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