A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150706



Internal ID19197196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:64333758..64334062hg38UCSC Ensembl
Outerchr4:65199476..65199780hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996177
SamplesKWB1
Known GenesTECRL
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150706
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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