A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2850n106



Internal ID22796678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88601757..88602080hg38UCSC Ensembl
chr4:89522908..89523231hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1127327, nsv1113395
SamplesKWS1
Known GenesHERC3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2850n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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