A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953292



Internal ID17302166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:37127699..37132198hg38UCSC Ensembl
Outerchr19:37618601..37623100hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999828
SamplesBILGI_BIOE
Known GenesZNF420
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953292
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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