A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4368n106



Internal ID22798196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56829352..56829447hg38UCSC Ensembl
chrY:58975499..58975594hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1115321, nsv1110122
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4368n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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