A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766833



Internal ID18965924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3639058..3639759hg38UCSC Ensembl
chrX:3557099..3557800hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076242
Supporting Variants
SamplesKWP1
Known GenesPRKX
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766833
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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