A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3983205



Internal ID19225314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:92230242..92230300hg38UCSC Ensembl
Outerchr11:91963408..91963466hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145563
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3983205
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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