A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121093



Internal ID19272700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:24809152..24809490hg38UCSC Ensembl
Outerchr10:25098081..25098419hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv379n106
Supporting Variantsnssv3995264, nssv3964775
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121093
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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