A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957699



Internal ID17306572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:63080765..63082501hg38UCSC Ensembl
Outerchr9:66985737..66987473hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg381737
hg191737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002310
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957699
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