A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768784



Internal ID19313145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:18350879..18355580hg38UCSC Ensembl
chrX:18368999..18373700hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg384702
hg194702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075309
Supporting Variants
SamplesKWP1
Known GenesSCML2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768784
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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