A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1116537



Internal ID18903604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:88805688..88805762hg38UCSC Ensembl
Outerchr4:89726839..89726913hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978719
SamplesKWS2
Known GenesFAM13A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1116537
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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