A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1127178



Internal ID19284877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:45790278..45790336hg38UCSC Ensembl
Outerchr11:45811829..45811887hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985552
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1127178
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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