A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3954713



Internal ID18878587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:104872296..104872493hg38UCSC Ensembl
Outerchr14:105338633..105338830hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1108924
Supporting Variants
SamplesKWS1
Known GenesCEP170B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3954713
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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