A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011735



Internal ID19100953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:5045629..5060550hg38UCSC Ensembl
Innerchr3:5087314..5102235hg19UCSC Ensembl
Innerchr3:5062314..5077235hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3814922
hg1914922
hg1814922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3591636
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)nsv1011735
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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