A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955512



Internal ID16957699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:47449153..47451947hg38UCSC Ensembl
Outerchr3:47490643..47493437hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg382795
hg192795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv125n73
Supporting Variantsnssv3004432
SamplesBILGI_BIOE
Known GenesSCAP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955512
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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