A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3992645



Internal ID18862806
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 StatusS
Merged Variantsnsv1141138
Supporting Variants
SamplesKWS1
Known GenesALKBH3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3992645
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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