A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110892



Internal ID19251042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:25565490..25596915hg38UCSC Ensembl
Outerchr12:25718424..25749849hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3831426
hg1931426
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961306
SamplesKWS1
Known GenesIFLTD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110892
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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