A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998856



Internal ID19158393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:68671304..68698250hg38UCSC Ensembl
Innerchr3:68720455..68747401hg19UCSC Ensembl
Innerchr3:68803145..68830091hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3826947
hg1926947
hg1826947
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4771n100
Supporting Variantsnssv3594017, nssv3732978, nssv3594019, nssv3594033, nssv3594024, nssv3594051, nssv3732977, nssv3594028, nssv3594025, nssv3594049, nssv3594022, nssv3594047, nssv3594021, nssv3594029, nssv3594020, nssv3594031, nssv3594050, nssv3594015, nssv3594018, nssv3594038, nssv3594040, nssv3594023, nssv3594032, nssv3594043, nssv3594044, nssv3594030, nssv3594045, nssv3594036, nssv3594016, nssv3594035, nssv3594034, nssv3594042, nssv3594041, nssv3594039, nssv3594037, nssv3594048, nssv3594027, nssv3594026, nssv3594046
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998856
Frequency
Sample Size11257
Observed Gain9
Observed Loss30
Observed Complex0
Frequencyn/a


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