A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060341



Internal ID19149560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53426511..53503054hg38UCSC Ensembl
Innerchr19:53929764..54006308hg19UCSC Ensembl
Innerchr19:58621576..58698120hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3876544
hg1976545
hg1876545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3649n100
Supporting Variantsnssv3573260
Samples
Known GenesTPM3P9, ZNF761, ZNF813
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060341
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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