A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052973



Internal ID19142192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12094235..12214023hg38UCSC Ensembl
Innerchr16:12188092..12307880hg19UCSC Ensembl
Innerchr16:12095593..12215381hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38119789
hg19119789
hg18119789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557144
Samples
Known GenesSNX29
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052973
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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