A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3992669



Internal ID19225396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:72142458..72181192hg38UCSC Ensembl
Outerchr11:71853502..71892236hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3838735
hg1938735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1141161
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3992669
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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