A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956377



Internal ID16958564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:85739620..85739923hg38UCSC Ensembl
Outerchr4:86660773..86661076hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3005223
SamplesBILGI_BIOE
Known GenesARHGAP24
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956377
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