A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115903



Internal ID18925641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:8563335..8564972hg38UCSC Ensembl
Outerchr16:8613337..8614974hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg381638
hg191638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978465
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115903
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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