A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997073



Internal ID16943339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:3063409..3069608hg38UCSC Ensembl
Outerchr10:3105601..3111800hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951237
Supporting Variants
SamplesBILGI_BIOE
Known GenesPFKP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997073
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