A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6887736



Internal ID9935934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:7751869..7752080hg38UCSC Ensembl
Outerchr10:7793832..7794043hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2732406, esv2732395, esv2732384
Supporting Variants
SamplesSSM096
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)essv6887736
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