A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4367n106



Internal ID22798195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26638053..26672953hg38UCSC Ensembl
chrY:28784200..28819100hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3834901
hg1934901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1115947, nsv1132816
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4367n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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