A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv988562



Internal ID16282518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2383657..2420546hg38UCSC Ensembl
Innerchr4:2385384..2422273hg19UCSC Ensembl
Innerchr4:2355182..2392071hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3836890
hg1936890
hg1836890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593403
Supporting Variants
Samples
Known GenesLOC402160, ZFYVE28
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv988562
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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