A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565784



Internal ID16353193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100589943..100646193hg38UCSC Ensembl
Innerchr14:101056280..101112530hg19UCSC Ensembl
Innerchr14:100126033..100182283hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3856251
hg1956251
hg1856251
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv833077
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565784
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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