A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044973



Internal ID19134192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4069057..4106856hg38UCSC Ensembl
Innerchr16:4119058..4156857hg19UCSC Ensembl
Innerchr16:4059059..4096858hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3837800
hg1937800
hg1837800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3556971
Samples
Known GenesADCY9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044973
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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