A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953573



Internal ID16955760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:39444461..39522960hg38UCSC Ensembl
Outerchr19:39935101..40013600hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3878500
hg1978500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999839
SamplesBILGI_BIOE
Known GenesDLL3, SELV, SUPT5H, TIMM50
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953573
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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