A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112495



Internal ID19281073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93874469..93880102hg38UCSC Ensembl
Outerchr11:93607635..93613268hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg385634
hg195634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984357, nssv3968365
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112495
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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