A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001634



Internal ID19090851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176170259..176215147hg38UCSC Ensembl
Innerchr3:175888047..175932935hg19UCSC Ensembl
Innerchr3:177370741..177415629hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3844889
hg1944889
hg1844889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3738446
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)nsv1001634
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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