A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960927



Internal ID19203950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:74548550..74548609hg38UCSC Ensembl
Outerchr8:75460785..75460844hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120167
Supporting Variants
SamplesKWS1
Known GenesMIR5681A, MIR5681B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960927
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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