A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077367



Internal ID18977949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63239693..63242475hg38UCSC Ensembl
chr1:63705364..63708146hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg382783
hg192783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765246
SamplesKWP1
Known GenesLINC00466
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077367
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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