A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987814



Internal ID18859007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:170141172..170265223hg38UCSC Ensembl
Outerchr6:170456396..170574311hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38124052
hg19117916
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133017
Supporting Variants
SamplesKWS1
Known GenesLOC154449
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987814
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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