A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132337



Internal ID18911161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46398162..46602717hg38UCSC Ensembl
Outerchr10:46946900..47151600hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38204556
hg19204701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv440n106
Supporting Variantsnssv3987109
SamplesKWS1
Known GenesGPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, SYT15
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132337
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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