A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953975



Internal ID16956162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:11412925..11424131hg38UCSC Ensembl
Outerchr19:11523601..11534800hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3811207
hg1911200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998952
SamplesBILGI_BIOE
Known GenesCCDC151, RGL3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953975
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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