A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3954665



Internal ID18862487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:11319873..11319941hg38UCSC Ensembl
Outerchr19:11430549..11430617hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116300
Supporting Variants
SamplesKWS1
Known GenesTSPAN16
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3954665
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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