A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999492



Internal ID19190119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:26961168..26961564hg38UCSC Ensembl
Outerchr1:27287659..27288055hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38397
hg19397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1146291
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999492
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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