A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4356n106



Internal ID22798184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11677894..11721494hg38UCSC Ensembl
chrY:13798600..13842200hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3843601
hg1943601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1110645, nsv1125157
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4356n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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