A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110695



Internal ID21293961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:6537937..7300290hg38UCSC Ensembl
InnerchrX:6455978..7218331hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38762354
hg19762354
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101832
Samplessample403
Known GenesHDHD1, MIR4767, STS
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110695
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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