A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110181



Internal ID19285184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:125886031..125918331hg38UCSC Ensembl
Outerchr10:127574600..127606900hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3832301
hg1932301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv531n106
Supporting Variantsnssv3959448
SamplesKWS1
Known GenesFANK1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110181
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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