A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036814



Internal ID19126033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14324465..14385913hg38UCSC Ensembl
Innerchr16:14418322..14479770hg19UCSC Ensembl
Innerchr16:14325823..14387271hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3861449
hg1961449
hg1861449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557234
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)nsv1036814
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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