A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3972639



Internal ID19237518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:15616101..15616194hg38UCSC Ensembl
Outerchr19:15726912..15727005hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134756
Supporting Variants
SamplesKWS2
Known GenesCYP4F8
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3972639
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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