A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110915



Internal ID19251367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:59656096..59674933hg38UCSC Ensembl
Outerchr16:59690000..59708837hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3818838
hg1918838
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961332
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110915
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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