A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124611



Internal ID19265022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:5369837..5371537hg38UCSC Ensembl
Outerchr10:5411800..5413500hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381701
hg191701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv351n106
Supporting Variantsnssv3976665
SamplesKWS2
Known GenesUCN3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124611
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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