A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122297



Internal ID18934660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:11148657..11148726hg38UCSC Ensembl
Outerchr1:11208714..11208783hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969748
SamplesKWS2
Known GenesMTOR, MTOR-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122297
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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