A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3993387



Internal ID19233509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:9311683..9420183hg38UCSC Ensembl
Outerchr12:9464279..9572779hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38108501
hg19108501
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1141880
Supporting Variants
SamplesKWS2
Known GenesDDX12P, LOC642846
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3993387
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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