A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997028



Internal ID17289980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:134908755..134915654hg38UCSC Ensembl
Outerchr9:137800601..137807500hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951816
Supporting Variants
SamplesBILGI_BIOE
Known GenesFCN1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997028
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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