A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150426



Internal ID19197478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:26495599..26495693hg38UCSC Ensembl
Outerchr22:26891565..26891659hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003725
SamplesKWB1
Known GenesTFIP11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150426
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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