A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055862



Internal ID18798393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83162346..83178793hg38UCSC Ensembl
Innerchr16:83195951..83212398hg19UCSC Ensembl
Innerchr16:81753452..81769899hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3816448
hg1916448
hg1816448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3053n100
Supporting Variantsnssv3719106
Samples
Known GenesCDH13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055862
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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