A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969153



Internal ID18886852
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 StatusS
Merged Variantsnsv1133589
Supporting Variants
SamplesKWS2
Known GenesKLHL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969153
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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