A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125330



Internal ID18929719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:13063021..13063277hg38UCSC Ensembl
Outerchr10:13105021..13105277hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38257
hg19257
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987791, nssv3978674
SamplesKWS1, KWS2
Known GenesCCDC3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125330
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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