A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000599



Internal ID16946865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:29423228..29423780hg38UCSC Ensembl
Outerchr10:29712157..29712709hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv955621
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000599
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