A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101832



Internal ID21287561
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 StatusS
Merged Variantsnsv3110695
Supporting Variants
Samplessample403
Known GenesHDHD1, MIR4767, STS
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101832
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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