A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110901



Internal ID19262512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:78066932..78077552hg38UCSC Ensembl
Outerchr13:78641067..78651687hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3810621
hg1910621
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961317
SamplesKWS1
Known GenesRNF219-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110901
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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