A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120079



Internal ID18924128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:22562266..22578645hg38UCSC Ensembl
Outerchr10:22851195..22867574hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3816380
hg1916380
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960823
SamplesKWS1
Known GenesPIP4K2A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120079
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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