A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067528



Internal ID19156747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42776064..42864771hg38UCSC Ensembl
Innerchr19:43280216..43368923hg19UCSC Ensembl
Innerchr19:47972056..48060763hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3888708
hg1988708
hg1888708
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3562n100
Supporting Variantsnssv3568897
Samples
Known GenesLOC100289650, PSG10P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067528
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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