A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957487



Internal ID17306360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:50073398..50074953hg38UCSC Ensembl
Outerchr14:50540116..50541671hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg381556
hg191556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004366
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957487
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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