A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970091



Internal ID18883237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:39502436..39502508hg38UCSC Ensembl
Outerchr19:39993076..39993148hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1114009
Supporting Variants
SamplesKWS2
Known GenesDLL3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970091
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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