A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4358n106



Internal ID22798186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:13114086..13120686hg38UCSC Ensembl
chrY:15226000..15232600hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg386601
hg196601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1144331, nsv1113051
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4358n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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