A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956575



Internal ID16958762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:14621501..14623298hg38UCSC Ensembl
Outerchr19:14732313..14734110hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381798
hg191798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002826
SamplesBILGI_BIOE
Known GenesEMR3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956575
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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