A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132982



Internal ID18916157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:112867074..112867147hg38UCSC Ensembl
Outerchr9:115629354..115629427hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987776
SamplesKWS1
Known GenesSNX30
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132982
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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