A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055495



Internal ID19144714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42776064..42882021hg38UCSC Ensembl
Innerchr19:43280216..43386173hg19UCSC Ensembl
Innerchr19:47972056..48078013hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38105958
hg19105958
hg18105958
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3555n100
Supporting Variantsnssv3568899
Samples
Known GenesLOC100289650, PSG1, PSG10P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055495
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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