A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976461



Internal ID19209457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:118875623..118875709hg38UCSC Ensembl
Outerchr11:118746332..118746418hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115408
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976461
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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