A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578618



Internal ID16019341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11809400..11903459hg38UCSC Ensembl
Innerchr19:11920215..12014274hg19UCSC Ensembl
Innerchr19:11781215..11875274hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3894060
hg1994060
hg1894060
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150643
Samples1780846321_A
Known GenesZNF439, ZNF440, ZNF69
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578618
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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