A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572844



Internal ID16013567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:61625455..61690440hg38UCSC Ensembl
Innerchr16:61659359..61724344hg19UCSC Ensembl
Innerchr16:60216860..60281845hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3864986
hg1964986
hg1864986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv858914
Samples
Known GenesCDH8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572844
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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