A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956563



Internal ID16958750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:36349824..36356185hg38UCSC Ensembl
Outerchr19:36840726..36847087hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg386362
hg196362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv83n73
Supporting Variantsnssv3002814
SamplesBILGI_BIOE
Known GenesZFP14
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956563
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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