A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125367



Internal ID19258819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:20566648..20566714hg38UCSC Ensembl
Outerchr16:20577970..20578036hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1314n106
Supporting Variantsnssv3983541
SamplesKWS2
Known GenesACSM2B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125367
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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