A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950898



Internal ID17299772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:93287419..93308918hg38UCSC Ensembl
Outerchr9:96049701..96071200hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3821500
hg1921500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996931
SamplesBILGI_BIOE
Known GenesWNK2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950898
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