A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065962



Internal ID19155181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42751053..42870449hg38UCSC Ensembl
Innerchr19:43255205..43374601hg19UCSC Ensembl
Innerchr19:47947045..48066441hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38119397
hg19119397
hg18119397
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3555n100
Supporting Variantsnssv3722858, nssv3722859, nssv3722860, nssv3568807, nssv3568808, nssv3568809
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065962
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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