A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957724



Internal ID17306597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:133549028..133549349hg38UCSC Ensembl
Outerchr9:136414150..136414471hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002334
SamplesBILGI_BIOE
Known GenesADAMTSL2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957724
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