A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978754



Internal ID19243590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:130897690..130898322hg38UCSC Ensembl
Outerchr8:131909936..131910568hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1142034
Supporting Variants
SamplesKWS2
Known GenesADCY8
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978754
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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