A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059154



Internal ID19148373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89761992..89820143hg38UCSC Ensembl
Innerchr16:89828400..89886551hg19UCSC Ensembl
Innerchr16:88355901..88414052hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3858152
hg1958152
hg1858152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560008
Samples
Known GenesFANCA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059154
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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