A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3636399



Internal ID18587994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:187530002..188872654hg38UCSC Ensembl
Innerchr4:188451156..189793808hg19UCSC Ensembl
Innerchr4:188688150..190030802hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg381342653
hg191342653
hg181342653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017684
Supporting Variants
Samples
Known GenesLINC01060, TRIML1, TRIML2, ZFP42
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3636399
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