A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137485



Internal ID18936401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:97589317..97589376hg38UCSC Ensembl
Outerchr9:100351599..100351658hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3976932
SamplesKWS2
Known GenesTMOD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137485
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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