A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4339n106



Internal ID20163696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:6240159..6266359hg38UCSC Ensembl
chrY:6108200..6134400hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3826201
hg1926201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1119383, nsv1140092
SamplesKWS2, KWS1
Known GenesTSPY2, TTTY23, TTTY23B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4339n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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