A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111919



Internal ID19259537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:49491725..49491871hg38UCSC Ensembl
Outerchr14:49958443..49958589hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1080n106
Supporting Variantsnssv3964366, nssv3970898
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111919
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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