A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1068705



Internal ID18971453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171095858..171096659hg38UCSC Ensembl
chr1:171064999..171065800hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765410
SamplesKWP1
Known GenesFMO3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1068705
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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