A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4277n106



Internal ID22798105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:114720791..114726191hg38UCSC Ensembl
chrX:113955200..113960600hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg385401
hg195401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1129092, nsv1141700
SamplesKWS2, KWS1
Known GenesHTR2C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4277n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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