A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120660



Internal ID18910013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:74821378..74821678hg38UCSC Ensembl
Outerchr11:74532423..74532723hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv676n106
Supporting Variantsnssv3963091
SamplesKWS2
Known GenesRNF169
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120660
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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