A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126244



Internal ID19263454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:17914971..17932571hg38UCSC Ensembl
Outerchr10:18203900..18221500hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3817601
hg1917601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984477
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126244
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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