A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958618



Internal ID16960805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:106725142..106725432hg38UCSC Ensembl
Outerchr11:106595868..106596158hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002609
SamplesBILGI_BIOE
Known GenesGUCY1A2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958618
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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