A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132838



Internal ID18906093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:15229583..15229665hg38UCSC Ensembl
Outerchr10:15271582..15271664hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987631
SamplesKWS1
Known GenesFAM171A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132838
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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