A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578385



Internal ID16019108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:2224388..2336009hg38UCSC Ensembl
Innerchr19:2224387..2336008hg19UCSC Ensembl
Innerchr19:2175387..2287008hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38111622
hg19111622
hg18111622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6218n54
Supporting Variantsnssv892073
Samples
Known GenesAMH, C19orf35, DOT1L, JSRP1, LINGO3, LSM7, MIR1227, MIR4321, MIR6789, OAZ1, PLEKHJ1, SF3A2, SPPL2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578385
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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