A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036125



Internal ID18778656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8670288..8704399hg38UCSC Ensembl
Innerchr16:8764145..8798256hg19UCSC Ensembl
Innerchr16:8671646..8705757hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3834112
hg1934112
hg1834112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557106
Samples
Known GenesABAT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036125
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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