A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3974485



Internal ID19242154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:138135188..138135248hg38UCSC Ensembl
Outerchr4:139056342..139056402hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1114574
Supporting Variants
SamplesKWS2
Known GenesSLC7A11-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3974485
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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