A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961312



Internal ID18868480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:120344818..120344891hg38UCSC Ensembl
Outerchr12:120782621..120782694hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110897
Supporting Variants
SamplesKWS1
Known GenesMSI1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961312
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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