A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968974



Internal ID18896486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:64396874..64396941hg38UCSC Ensembl
Outerchr14:64863592..64863659hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113658
Supporting Variants
SamplesKWS2
Known GenesMIR548AZ, MTHFD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968974
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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