A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987846



Internal ID19204510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:12928174..12928255hg38UCSC Ensembl
Outerchr12:13081108..13081189hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133040
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987846
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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