A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953283



Internal ID16955470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:35247998..35314097hg38UCSC Ensembl
Outerchr19:35738901..35805000hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3866100
hg1966100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999819
SamplesBILGI_BIOE
Known GenesHAMP, LSR, MAG, USF2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953283
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