A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144141



Internal ID18915168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:41546162..41547362hg38UCSC Ensembl
Outerchr6:41513900..41515100hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994864
SamplesKWS1
Known GenesFOXP4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144141
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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