A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996975



Internal ID17289927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:126326622..126327321hg38UCSC Ensembl
Outerchr9:129088901..129089600hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951763
Supporting Variants
SamplesBILGI_BIOE
Known GenesMVB12B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2996975
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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