A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978638



Internal ID18897887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:117134526..117210001hg38UCSC Ensembl
Outerchr11:117005242..117080717hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3875476
hg1975476
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116457
Supporting Variants
SamplesKWS2
Known GenesLOC100652768, PAFAH1B2, PCSK7, SIDT2, TAGLN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978638
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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