A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063412



Internal ID18805943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82773048..82792902hg38UCSC Ensembl
Innerchr16:82806653..82826507hg19UCSC Ensembl
Innerchr16:81364154..81384008hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3819855
hg1919855
hg1819855
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559856
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)nsv1063412
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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