A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3965080



Internal ID18898865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:72093673..72095814hg38UCSC Ensembl
Outerchr15:72386014..72388155hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382142
hg192142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129942
Supporting Variants
SamplesKWS2
Known GenesMYO9A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3965080
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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