A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063445



Internal ID19152664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42790226..43020166hg38UCSC Ensembl
Innerchr19:43294378..43524318hg19UCSC Ensembl
Innerchr19:47986218..48216158hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38229941
hg19229941
hg18229941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3558n100
Supporting Variantsnssv3571622, nssv3722911, nssv3571623, nssv3571629, nssv3571630, nssv3571627, nssv3571626, nssv3571624, nssv3571625, nssv3571621, nssv3571632, nssv3571631, nssv3571633, nssv3571628
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, 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)nsv1063445
Frequency
Sample Size11257
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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