A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2933n106



Internal ID20162290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165207448..165208148hg38UCSC Ensembl
chr4:166128600..166129300hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1126702, nsv1133589
SamplesKWS2, KWS1
Known GenesKLHL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2933n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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