A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989377



Internal ID18884312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:125426549..125426682hg38UCSC Ensembl
Outerchr11:125296445..125296578hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1135789
Supporting Variants
SamplesKWS2
Known GenesPKNOX2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989377
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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