A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113330



Internal ID19249765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:93785720..93786738hg38UCSC Ensembl
Outerchr10:95545477..95546495hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg381019
hg191019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv501n106
Supporting Variantsnssv3964903, nssv3970759
SamplesKWS2, KWS1
Known GenesLGI1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113330
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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