A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132204



Internal ID18927074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69137248..69137310hg38UCSC Ensembl
Outerchr9:71752164..71752226hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3986938
SamplesKWS1
Known GenesTJP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132204
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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