A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953625



Internal ID16955812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:55637035..55699834hg38UCSC Ensembl
Outerchr19:56148401..56211200hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3862800
hg1962800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999891
SamplesBILGI_BIOE
Known GenesCCDC106, EPN1, U2AF2, ZNF580, ZNF581
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953625
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