A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970110



Internal ID18891648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:49825754..49825821hg38UCSC Ensembl
Outerchr19:50329011..50329078hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1114025
Supporting Variants
SamplesKWS2
Known GenesMED25
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970110
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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