A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2717977



Internal ID9952268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:3937398..3937692hg38UCSC Ensembl
Outerchr19:3937396..3937690hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6832250
SamplesSSM081
Known GenesNMRK2
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2717977
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer