A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4232n106



Internal ID22798060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42888751..42892851hg38UCSC Ensembl
chrX:42748000..42752100hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg384101
hg194101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1110601, nsv1140025
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4232n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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