A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523445



Internal ID15450738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:93155075..93174103hg38UCSC Ensembl
Innerchr14:93621420..93640448hg19UCSC Ensembl
Innerchr14:92691173..92710201hg18UCSC Ensembl
Innerchr14:92691173..92710201hg17UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3819029
hg1919029
hg1819029
hg1719029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699201
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523445
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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