A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141177



Internal ID18929767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46395862..46635417hg38UCSC Ensembl
Outerchr10:46914200..47153900hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38239556
hg19239701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv440n106
Supporting Variantsnssv3992684
SamplesKWS2
Known GenesFAM35BP, GPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, SYT15
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141177
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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