A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981646



Internal ID18860107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:38663479..38664279hg38UCSC Ensembl
Outerchr4:38665100..38665900hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145029
Supporting Variants
SamplesKWS1
Known GenesFLJ13197, KLF3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981646
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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