A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4217n106



Internal ID22798045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:25929822..25930163hg38UCSC Ensembl
chrX:25947939..25948280hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1124495, nsv1132119
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4217n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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