A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119574



Internal ID18902534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:13063116..13063402hg38UCSC Ensembl
Outerchr10:13105116..13105402hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv367n106
Supporting Variantsnssv3960774
SamplesKWS1
Known GenesCCDC3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119574
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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