A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4342n106



Internal ID20163699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:10134491..10217991hg38UCSC Ensembl
chrY:9972100..10055600hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3883501
hg1983501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1115931, nsv1110641
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4342n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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