A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952425



Internal ID17301299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:19332892..19357891hg38UCSC Ensembl
Outerchr19:19443701..19468700hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3825000
hg1925000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998975
SamplesBILGI_BIOE
Known GenesMAU2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952425
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