A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953268



Internal ID17302142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:29385494..29423993hg38UCSC Ensembl
Outerchr19:29876401..29914900hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3838500
hg1938500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999804
SamplesBILGI_BIOE
Known GenesLOC284395
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953268
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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