A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109283



Internal ID18903802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:33203706..33204012hg38UCSC Ensembl
Outerchr10:33492634..33492940hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv393n106
Supporting Variantsnssv3955938
SamplesKWS1
Known GenesNRP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109283
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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