A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996997



Internal ID16943263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:129664622..129668921hg38UCSC Ensembl
Outerchr9:132426901..132431200hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951785
Supporting Variants
SamplesBILGI_BIOE
Known GenesPRRX2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2996997
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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