A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3983479



Internal ID19233512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:20468936..20556259hg38UCSC Ensembl
Outerchr16:20480258..20567581hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3887324
hg1987324
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125307
Supporting Variants
SamplesKWS2
Known GenesACSM2A, ACSM2B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3983479
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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