A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968962



Internal ID18897012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:45119491..45119559hg38UCSC Ensembl
Outerchr14:45588694..45588762hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113644
Supporting Variants
SamplesKWS2
Known GenesFKBP3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968962
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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