A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4264n106



Internal ID22798092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:87821200..87827000hg38UCSC Ensembl
chrX:87076200..87082000hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg385801
hg195801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1110612, nsv1115877
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4264n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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