A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2871n106



Internal ID22796699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107053163..107053330hg38UCSC Ensembl
chr4:107974320..107974487hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1111650, nsv1112075
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2871n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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