A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110567



Internal ID18905172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:40933171..41129571hg38UCSC Ensembl
Outerchr9:69006400..69202800hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38196401
hg19196401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960221
SamplesKWS1
Known GenesFOXD4L6, LOC440896, PGM5P2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110567
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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