A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6718221



Internal ID9786442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:91159234..91159498hg38UCSC Ensembl
Outerchr1:91624791..91625055hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2714684, esv2714696
Supporting Variants
SamplesSSM044
Known Genes
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)essv6718221
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