A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960844



Internal ID19215267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:26481990..26482372hg38UCSC Ensembl
Outerchr13:27056127..27056509hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120096
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960844
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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