A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047701



Internal ID19136920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:13389452..13594055hg38UCSC Ensembl
Innerchr16:13483309..13687912hg19UCSC Ensembl
Innerchr16:13390810..13595413hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38204604
hg19204604
hg18204604
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718890
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)nsv1047701
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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