A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4272n106



Internal ID22798100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:110816972..110822272hg38UCSC Ensembl
chrX:110060200..110065500hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg385301
hg195301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1132780, nsv1125119
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4272n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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