A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951523



Internal ID16953710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69123185..69128584hg38UCSC Ensembl
Outerchr9:71738101..71743500hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996902
SamplesBILGI_BIOE
Known GenesTJP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951523
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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