A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041381



Internal ID19130600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12631132..12657939hg38UCSC Ensembl
Innerchr16:12724989..12751796hg19UCSC Ensembl
Innerchr16:12632490..12659297hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3826808
hg1926808
hg1826808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718884
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)nsv1041381
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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