A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143811



Internal ID18925789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:14688343..14723343hg38UCSC Ensembl
Outerchr16:14782200..14817200hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3835001
hg1935001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994507
SamplesKWS1
Known GenesNPIPA2, NPIPA3, PLA2G10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143811
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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