A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001885



Internal ID18744416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:4080615..4318741hg38UCSC Ensembl
Innerchr4:4082342..4320468hg19UCSC Ensembl
Innerchr4:4133243..4371369hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38238127
hg19238127
hg18238127
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3616170
Samples
Known GenesLYAR, OTOP1, TMEM128, ZBTB49
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001885
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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