A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950936



Internal ID16953123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:120855623..120877422hg38UCSC Ensembl
Outerchr9:123617901..123639700hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3821800
hg1921800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996965
SamplesBILGI_BIOE
Known GenesPHF19
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950936
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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