A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955318



Internal ID16957505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:14126901..14142100hg38UCSC Ensembl
Outerchr3:14168401..14183600hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3815200
hg1915200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001338
SamplesBILGI_BIOE
Known GenesTMEM43
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955318
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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