A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578277



Internal ID16019000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1249512..1250886hg38UCSC Ensembl
Innerchr19:1249511..1250885hg19UCSC Ensembl
Innerchr19:1200511..1201885hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381375
hg191375
hg181375
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6198n54
Supporting Variantsnssv891782
Samples
Known GenesMIDN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578277
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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