A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv880884



Internal ID6287895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:175440024..175445237hg19UCSC Ensembl
Outerchr4:175439056..175453830hg19UCSC Ensembl
Innerchr4:175676599..175681812hg18UCSC Ensembl
Outerchr4:175675631..175690405hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1507987
SamplesSP54684
Known GenesHPGD
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv880884
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer