A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057735



Internal ID19146954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42857538..43199340hg38UCSC Ensembl
Innerchr19:43361690..43703492hg19UCSC Ensembl
Innerchr19:48053530..48395332hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38341803
hg19341803
hg18341803
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3557n100
Supporting Variantsnssv3723026
Samples
Known GenesPSG1, 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)nsv1057735
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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