A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3972629



Internal ID18895609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:6663361..6663427hg38UCSC Ensembl
Outerchr19:6663372..6663438hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134749
Supporting Variants
SamplesKWS2
Known GenesTNFSF14
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3972629
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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