A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578665



Internal ID16019388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14620874..14623091hg38UCSC Ensembl
Innerchr19:14731686..14733903hg19UCSC Ensembl
Innerchr19:14592686..14594903hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382218
hg192218
hg182218
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv894844, nssv894846, nssv894845
Samples
Known GenesEMR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578665
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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