A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1068324



Internal ID19320273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6218975..6220368hg38UCSC Ensembl
chrX:6137016..6138409hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg381394
hg191394
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770678
SamplesKWP1
Known GenesNLGN4X
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1068324
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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