A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122489



Internal ID18914320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:11085524..11085577hg38UCSC Ensembl
Outerchr10:11127487..11127540hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970691
SamplesKWS2
Known GenesCELF2, CELF2-AS2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122489
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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