A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956562



Internal ID16958749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:54052306..54057474hg38UCSC Ensembl
Outerchr19:54555560..54560728hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg385169
hg195169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002813
SamplesBILGI_BIOE
Known GenesVSTM1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956562
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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