A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999564



Internal ID19159101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3584513..3707900hg38UCSC Ensembl
Innerchr4:3586240..3709627hg19UCSC Ensembl
Innerchr4:3556038..3679425hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38123388
hg19123388
hg18123388
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5083n100
Supporting Variantsnssv3616118
Samples
Known GenesLINC00955, LOC100133461
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999564
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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