A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1068426



Internal ID18971398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202955444..202955611hg38UCSC Ensembl
chr1:202924572..202924739hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3773011
SamplesKWP1
Known GenesADIPOR1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1068426
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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