A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2180n106



Internal ID22796008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237211557..237213457hg38UCSC Ensembl
chr2:238120200..238122100hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg381901
hg191901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1139747, nsv1110363
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2180n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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