A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962802



Internal ID19217370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:45763196..45781372hg38UCSC Ensembl
Outerchr12:46156979..46175155hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3818177
hg1918177
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129365
Supporting Variants
SamplesKWS1
Known GenesARID2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962802
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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