A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150507



Internal ID18849258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:155733561..155736439hg38UCSC Ensembl
Outerchr4:156654713..156657591hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg382879
hg192879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3995983
SamplesKWB1
Known GenesGUCY1A3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150507
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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