A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4218n106



Internal ID22798046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26312883..26319383hg38UCSC Ensembl
chrX:26331000..26337500hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg386501
hg196501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1125085, nsv1132756
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4218n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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