A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135369



Internal ID19252520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:165081448..165083948hg38UCSC Ensembl
Outerchr4:166002600..166005100hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg382501
hg192501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2932n106
Supporting Variantsnssv3988929
SamplesKWS2
Known GenesTMEM192
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135369
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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