A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122583



Internal ID18903635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:9468898..9468966hg38UCSC Ensembl
Outerchr11:9490445..9490513hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970795
SamplesKWS2
Known GenesZNF143
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122583
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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