A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063388



Internal ID19152607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42798345..43193169hg38UCSC Ensembl
Innerchr19:43302497..43697321hg19UCSC Ensembl
Innerchr19:47994337..48389161hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38394825
hg19394825
hg18394825
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3557n100
Supporting Variantsnssv3569559
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG2, PSG4, PSG5, PSG6, PSG7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063388
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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