A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3983563



Internal ID19234851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:3620536..3627897hg38UCSC Ensembl
Outerchr20:3601183..3608544hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg387362
hg197362
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125392
Supporting Variants
SamplesKWS2
Known GenesATRN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3983563
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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