A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143812



Internal ID18903621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:16228343..16239443hg38UCSC Ensembl
Outerchr16:16322200..16333300hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3811101
hg1911101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994508
SamplesKWS1
Known GenesNOMO3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143812
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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