A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4371n106



Internal ID22798199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56831584..56836805hg38UCSC Ensembl
chrY:58977731..58982952hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg385222
hg195222
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1117926, nsv1111400
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4371n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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