A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056158



Internal ID18798689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83293409..83313074hg38UCSC Ensembl
Innerchr16:83327014..83346679hg19UCSC Ensembl
Innerchr16:81884515..81904180hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3819666
hg1919666
hg1819666
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3719108, nssv3719109
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)nsv1056158
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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