A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141138



Internal ID18923816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:43888075..43888363hg38UCSC Ensembl
Outerchr11:43909625..43909913hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv630n106
Supporting Variantsnssv3992645
SamplesKWS1
Known GenesALKBH3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141138
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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