A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6745932



Internal ID9652794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:20540092..20619351hg38UCSC Ensembl
Outerchr19:20722898..20802157hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3879260
hg1979260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718314
Supporting Variants
SamplesSSM007
Known GenesZNF737
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)essv6745932
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