A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572845



Internal ID16360254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:61710917..61788727hg38UCSC Ensembl
Innerchr16:61744821..61822631hg19UCSC Ensembl
Innerchr16:60302322..60380132hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3877811
hg1977811
hg1877811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv858915
Samples
Known GenesCDH8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572845
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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