A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141908



Internal ID18901072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:12825172..12825245hg38UCSC Ensembl
Outerchr10:12867171..12867244hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3993414
SamplesKWS2
Known GenesCAMK1D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141908
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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