A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126627



Internal ID18907591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:26589736..26590336hg38UCSC Ensembl
Outerchr22:26985700..26986300hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984890
SamplesKWS1
Known GenesTPST2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126627
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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