A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073591



Internal ID18973725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142317862..142318263hg38UCSC Ensembl
chr6:142638999..142639400hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767045
SamplesKWP1
Known GenesGPR126
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073591
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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