A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1131109



Internal ID19282530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:14353543..14354643hg38UCSC Ensembl
Outerchr16:14447400..14448500hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1301n106
Supporting Variantsnssv3967814
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1131109
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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