A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956816



Internal ID17305689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:18714287..18714631hg38UCSC Ensembl
Outerchr3:18755779..18756123hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004513
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956816
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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