A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3591636



Internal ID18889917
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 StatusS
Merged Variantsnsv1011735
Supporting Variants
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)nssv3591636
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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