A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1072632



Internal ID19318508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26901536..26903737hg38UCSC Ensembl
chr22:27297499..27299700hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg382202
hg192202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765564
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1072632
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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