A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134952



Internal ID18922432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:74821374..74821681hg38UCSC Ensembl
Outerchr11:74532419..74532726hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv676n106
Supporting Variantsnssv3988480
SamplesKWS1
Known GenesRNF169
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134952
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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