A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572902



Internal ID16013625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:66398520..66424956hg38UCSC Ensembl
Innerchr16:66432423..66458859hg19UCSC Ensembl
Innerchr16:64989924..65016360hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3826437
hg1926437
hg1826437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv859069
Samples
Known GenesCDH5, LINC00920
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572902
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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