A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2724n106



Internal ID20162081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7192373..7193073hg38UCSC Ensembl
chr4:7194100..7194800hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1118996, nsv1112850
SamplesKWS2, KWS1
Known GenesSORCS2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2724n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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