A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3971472



Internal ID19230375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:21656105..21656175hg38UCSC Ensembl
Outerchr14:22124321..22124391hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113622
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3971472
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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