A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112082



Internal ID18913320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:169229924..169230059hg38UCSC Ensembl
Outerchr4:170151075..170151210hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3965774
SamplesKWS2
Known GenesSH3RF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112082
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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