A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1108903



Internal ID19248708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:65038211..65038287hg38UCSC Ensembl
Outerchr14:65504929..65505005hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3954690
SamplesKWS1
Known GenesCHURC1-FNTB, FNTB, MAX
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1108903
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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