A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055454



Internal ID18797985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82931182..82950971hg38UCSC Ensembl
Innerchr16:82964787..82984576hg19UCSC Ensembl
Innerchr16:81522288..81542077hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3819790
hg1919790
hg1819790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3719088
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)nsv1055454
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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