A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955445



Internal ID16957632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:11768953..11769128hg38UCSC Ensembl
Outerchr18:11768952..11769127hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002806
SamplesBILGI_BIOE
Known GenesGNAL
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955445
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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