A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139388



Internal ID18925452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:3691430..3691485hg38UCSC Ensembl
OuterchrX:3609471..3609526hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960425, nssv3992560
SamplesKWS1, KWS2
Known GenesPRKX
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139388
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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