A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3991853



Internal ID18898184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:40339447..40339509hg38UCSC Ensembl
Outerchr4:40341464..40341526hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139233
Supporting Variants
SamplesKWS2
Known GenesCHRNA9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3991853
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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