A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997053



Internal ID17290005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:138211951..138231650hg38UCSC Ensembl
Outerchr9:141102401..141122100hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3819700
hg1919700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951217
Supporting Variants
SamplesBILGI_BIOE
Known GenesFAM157B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997053
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer