A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152321



Internal ID19195373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:99656799..99656884hg38UCSC Ensembl
Outerchr14:100123136..100123221hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996926
SamplesKWB1
Known GenesHHIPL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152321
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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