A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133589



Internal ID18926485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:165207448..165207948hg38UCSC Ensembl
Outerchr4:166128600..166129100hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2933n106
Supporting Variantsnssv3969153
SamplesKWS2
Known GenesKLHL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133589
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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