A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960931



Internal ID19208920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:127817522..127817592hg38UCSC Ensembl
Outerchr8:128829768..128829838hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120170
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960931
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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