A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951811



Internal ID17300685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:134589855..134595354hg38UCSC Ensembl
Outerchr9:137481701..137487200hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997023
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951811
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