A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998559



Internal ID16944825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:102256821..102325182hg38UCSC Ensembl
Outerchr7:101900101..101965600hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3868362
hg1965500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv949918
Supporting Variants
SamplesBILGI_BIOE
Known GenesCUX1, MIR4285, SH2B2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998559
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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