A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111791



Internal ID18927947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:27324879..27339879hg38UCSC Ensembl
Outerchr16:27336200..27351200hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3815001
hg1915001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1333n106
Supporting Variantsnssv3964700
SamplesKWS2
Known GenesIL4R
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111791
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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