A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990866



Internal ID19241962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:74931820..74931898hg38UCSC Ensembl
Outerchr14:75398523..75398601hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1138315
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990866
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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