A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077142



Internal ID19323452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67854053..67855154hg38UCSC Ensembl
chr9:67921499..67922600hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg381102
hg191102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764237
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077142
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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