A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1127933



Internal ID18934976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:94773964..94774242hg38UCSC Ensembl
Outerchr10:47088424..47088702hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv442n106
Supporting Variantsnssv3957322
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1127933
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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