A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058834



Internal ID18801365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29963127..30017898hg38UCSC Ensembl
Innerchr19:30454034..30508805hg19UCSC Ensembl
Innerchr19:35145874..35200645hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3854772
hg1954772
hg1854772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3510n100
Supporting Variantsnssv3566540, nssv3566539
Samples
Known GenesURI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058834
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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