A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978635



Internal ID19240987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1665614..1685679hg38UCSC Ensembl
Outerchr11:1686844..1706909hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3820066
hg1920066
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116454
Supporting Variants
SamplesKWS2
Known GenesFAM99A, FAM99B, MOB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978635
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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