A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6850622



Internal ID9902355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:7751872..7752079hg38UCSC Ensembl
Outerchr10:7793835..7794042hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2732406, esv2732395, esv2732384
Supporting Variants
SamplesSSM086
Known GenesKIN
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)essv6850622
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