A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953982



Internal ID16956169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:14758889..14781488hg38UCSC Ensembl
Outerchr19:14869701..14892300hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3822600
hg1922600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998959
SamplesBILGI_BIOE
Known GenesEMR2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953982
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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