A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022201



Internal ID18764735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:155657250..155676831hg38UCSC Ensembl
Innerchr4:156578402..156597983hg19UCSC Ensembl
Innerchr4:156797852..156817433hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3819582
hg1919582
hg1819582
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636133
Samples
Known GenesGUCY1A3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022201
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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