A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996986



Internal ID17289938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:128401522..128420221hg38UCSC Ensembl
Outerchr9:131163801..131182500hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3818700
hg1918700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951774
Supporting Variants
SamplesBILGI_BIOE
Known GenesCERCAM
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2996986
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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