A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134049



Internal ID18908758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:103337765..103338079hg38UCSC Ensembl
Outerchr10:105097522..105097836hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970387
SamplesKWS2
Known GenesPCGF6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134049
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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