A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999046



Internal ID19158582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:70500321..70527793hg38UCSC Ensembl
Innerchr3:70549472..70576944hg19UCSC Ensembl
Innerchr3:70632162..70659634hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3827473
hg1927473
hg1827473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3594154
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)nsv999046
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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