A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565209



Internal ID16352618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:76673921..76743056hg38UCSC Ensembl
Innerchr14:77140264..77209399hg19UCSC Ensembl
Innerchr14:76210017..76279152hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3869136
hg1969136
hg1869136
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv829560
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565209
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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